Multi-vital sign detector in an electronic medical records system

ABSTRACT

In one implementation, a device detects multiple vital signs from sensors such as a digital infrared sensor, a photoplethysmogram (PPG) sensor and at least one micro dynamic light scattering (mDLS) sensor, and thereafter in some implementations the vital signs are transmitted to, and stored by, an electronic medical record system.

RELATED APPLICATION

This application is a continuation-in-part of, and claims the benefit and priority under 35 U.S.C. 120 of U.S. Original patent application Ser. No. 15/436,807 filed 18 Feb. 2017, which is hereby incorporated by reference in its entirety.

FIELD

This disclosure relates generally to detecting multiple vital signs and communicating detected multiple vital signs to a medical records system.

BACKGROUND

Prior techniques of capturing multiple vital signs from human subjects have implemented problematic sensors and have been very cumbersome in terms of affixing the sensors to the patient, recording, storing and forwarding the vital signs to appropriate parties.

BRIEF DESCRIPTION

In one aspect, a device measures temperature, heart rate at rest, heart rate variability, respiration, SPO2, blood flow, blood pressure, total hemoglobin (SpHb), PVi, methemoglobin (SpMet), acoustic respiration rate (RRa), carboxyhemoglobin (SpCO), oxygen reserve index (ORi), oxygen content (SpOC), ECG and/or EEG of a human.

In another aspect, a device to estimate a body core temperature includes a microprocessor, a digital infrared sensor that is operably coupled to the microprocessor with no analog-to-digital converter being operably coupled between the digital infrared sensor and the microprocessor, the digital infrared sensor including a Faraday cage that surrounds a single thermopile sensor, a central processing unit, an analog-to-digital converter and a control block; wherein the microprocessor is configured to receive from the digital readout ports a digital signal that is representative of an infrared signal of a forehead temperature that is detected by the digital infrared sensor and some further aspects the microprocessor is configured to estimate the body core temperature from the digital signal that is representative of the infrared signal in reference to a plurality of tables that are stored in a memory that correlate the forehead temperature that is calibration-corrected and voltage-corrected to the body core temperature and a voltage-corrected ambient temperature.

Apparatus, systems, and methods of varying scope are described herein. In addition to the aspects and advantages described in this summary, further aspects and advantages will become apparent by reference to the drawings and by reading the detailed description that follows.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a block diagram of an overview of an electronic medical records (EMR) capture system, according to an implementation.

FIG. 2 is a block diagram of apparatus of an EMR capture system, according to an implementation in which an interoperability manager component manages all communications in the middle layer.

FIG. 3 is a block diagram of an overview of an electronic medical records capture system, according to an implementation.

FIG. 4 is a block diagram of a multi-vital sign system, according to an implementation.

FIG. 5 is a block diagram of a multi-vital sign system, according to an implementation.

FIG. 6 is a block diagram of a multi-parameter sensor box, according to an implementation.

FIG. 7 is a block diagram of a multi-parameter sensor box, according to an implementation.

FIG. 8 is a block diagram of a front end of a multi-vital-sign finger cuff, according to an implementation.

FIG. 9 is a block diagram of pneumatic system components that are internal to the multiparameter sensor box, according to an implementation.

FIG. 10 is a block diagram of a multi-vital sign system, according to an implementation.

FIG. 11 is a block diagram of a multi-vital sign system, according to an implementation.

FIG. 12 is a block diagram of a multi-vital sign system, according to an implementation.

FIG. 13 is a block diagram of a multi-vital sign system, according to an implementation.

FIG. 14 is a data flow diagram of the non-contact human multi-vital sign device, according to an implementation.

FIG. 15 is a display screen of the non-contact human multi-vital sign device indicating that signal quality from the sensors is below a predetermined minimum threshold, according to an implementation.

FIG. 16 is a display screen of the non-contact human multi-vital sign device indicating that signal quality from the sensors is at or above a predetermined minimum threshold, according to an implementation.

FIG. 17 is a display screen of the non-contact human multi-vital sign device showing results of successful multi-vital sign measurements, according to an implementation.

FIG. 18 is a block diagram of an apparatus to estimate a body core temperature from a forehead temperature sensed by an infrared sensor, according to an implementation.

FIG. 19-20 are block diagrams of an apparatus to derive an estimated body core temperature from one or more tables that are stored in a memory that correlate a calibration-corrected voltage-corrected object temperature to the body core temperature in reference to the corrected ambient temperature, according to an implementation.

FIG. 21 is a block diagram of a multi-vital-sign capture system that includes a digital infrared sensor, a biological vital sign generator and a temporal variation amplifier, according to an implementation.

FIG. 22 is a block diagram of a multi-vital-sign capture system that includes a no-touch electromagnetic sensor with no temporal variation amplifier, according to an implementation.

FIG. 23 is a block diagram of a multi-vital-sign capture system that includes a non-touch electromagnetic sensor and that detects biological vital-signs from images captured by a solid-state image transducer, according to an implementation.

FIG. 24 is a block diagram of an apparatus to generate a predictive analysis of vital signs, according to an implementation.

FIG. 25 is a block diagram of a thermometer that includes a digital infrared sensor with no other vital sign detection components, according to an implementation.

FIG. 26 is a block diagram of a digital infrared sensor, according to an implementation.

FIG. 27 is a block diagram of a system of interoperation device manager, according to an implementation.

FIG. 28 is a flowchart of a method to perform real time quality check on finger cuff data, according to an implementation.

FIG. 29 is a flowchart of a method to estimate a body core temperature from a digital infrared sensor, according to an implementation.

FIG. 30 is a flowchart of a method to display body core temperature color indicators, according to an implementation of three colors.

FIG. 31 is a flowchart of a method to manage power in a multi-vital-sign capture system having a digital infrared sensor, according to an implementation.

FIG. 32 is a flowchart of a method to estimate a body core temperature from a forehead temperature sensed by an infrared sensor, according to an implementation.

FIG. 33 is a flowchart of a method to derive an estimated body core temperature from one or more tables that are stored in a memory that correlates the calibrated object temperature to the body core temperature in reference to the corrected ambient temperature, according to an implementation.

FIG. 34 is a block diagram of an apparatus of variation amplification, according to an implementation.

FIG. 35 is a block diagram of an apparatus of variation amplification, according to an implementation.

FIG. 36 is a block diagram of an apparatus of variation amplification, according to an implementation.

FIG. 37 is a block diagram of an apparatus of variation amplification, according to an implementation.

FIG. 38 is a block diagram of an apparatus of variation amplification, according to an implementation.

FIG. 39 is a block diagram of an apparatus to generate and present any one of a number of biological vital signs from amplified motion, according to an implementation.

FIG. 40 is a block diagram of an apparatus of variation amplification, according to an implementation.

FIG. 41 is a block diagram of an apparatus of variation amplification, according to an implementation.

FIG. 42 is an apparatus that performs variation amplification to generate biological vital signs, according to an implementation.

FIG. 43 is a flowchart of a method of variation amplification, according to an implementation.

FIG. 44 is a flowchart of a method of variation amplification, according to an implementation that does not include a separate action of determining a temporal variation.

FIG. 45 is a flowchart of a method of variation amplification, according to an implementation.

FIG. 46 is a flowchart of a method of variation amplification, according to an implementation.

FIG. 47 is a flowchart of a method of variation amplification from which to generate and communicate biological vital signs, according to an implementation.

FIG. 48 is a flowchart of a method to estimate a body core temperature from an external source point in reference to a body core temperature correlation table, according to an implementation.

FIG. 49 is a flowchart of a method to estimate a body core temperature from an external source point and other measurements in reference to a body core temperature correlation table, according to an implementation.

FIG. 50 is a block diagram of a multi-vital-sign capture system, according to an implementation.

FIG. 51 is a block diagram of a solid-state image transducer, according to an implementation.

FIG. 52 is a block diagram of a communication subsystem, according to an implementation.

FIG. 53 is a block diagram of a non-contact human multi-vital sign device, according to an implementation.

FIG. 54-61 are drawings of various views of a multi-vital-sign finger cuff, according to an implementation.

FIG. 62-68 are drawings of various views of a multi-vital-sign capture system, according to an implementation.

FIG. 69 is an exploded view of a non-contact human multi-vital sign device, according to an implementation.

FIG. 70 is a block diagram of a multi-vital sign system, according to an implementation.

FIG. 71 is a block diagram of a multi-parameter sensor box, according to an implementation that is operable to couple to a finger sensor assembly.

FIG. 72 is a block diagram of a front end of a multi-vital-sign finger cuff, according to an implementation.

FIG. 73 is a block diagram of a multi-vital-sign device in a telemedicine system.

FIG. 74 is a block diagram of a multi-vital-sign system.

FIG. 75 is a block diagram of a multi-vital-sign device in a telemedicine system.

FIG. 76 is an isometric drawing of a multi-vital sign-capture device according to an implementation.

DETAILED DESCRIPTION

In the following detailed description, reference is made to the accompanying drawings that form a part hereof, and in which is shown by way of illustration specific implementations which may be practiced. These implementations are described in sufficient detail to enable those skilled in the art to practice the implementations, and it is to be understood that other implementations may be utilized and that logical, mechanical, electrical and other changes may be made without departing from the scope of the implementations. The following detailed description is, therefore, not to be taken in a limiting sense.

The detailed description is divided into eleven sections. In the first section, an overview is shown. In the second section, apparatus of an electronic medical records capture system are described. In the third section, implementations of apparatus of multi-vital-sign capture systems are described. In the fourth section, implementations of non-touch table-based temperature correlation thermometers are described. In the fifth section, implementations of interoperability device manager components of an EMR System are described. In the sixth section, methods of digital infrared sensors in multi-vital-sign capture systems are described. In the seventh section, implementations of apparatus of biological vital sign variation amplification detectors are described. In the eighth section, implementations of methods of biological vital sign amplification are described. In the ninth section, implementations of methods of non-touch table-based temperature correlation are described. In the tenth section, hardware and operating environments in which implementations may be practiced are described. Finally, in the eleventh section, a conclusion of the detailed description is provided.

1. Overview

FIG. 1 is a block diagram of apparatus of an electronic medical records (EMR) capture system 100, according to an implementation.

EMR capture system 100 includes a device/user layer 102 that further includes one or more multi-vital-sign capture system(s) 104. Examples of the multi-vital-sign capture system(s) 104 are shown in FIG. 4-14.

EMR capture system 100 includes a middle layer 106 that communicates with the multi-vital-sign capture system(s) 104 in the device/user layer 102. The middle layer 106 includes user/patient vital sign results data 108 that is communicated via cellular communication paths, such as 3G, 4G or a 5G or a WiFi® communication path, user/patient vital sign results data 110 that is communicated via a WiFi® communication path and user/patient vital sign results data 112 that is communicated via a Bluetooth® communication path. The middle layer 106 further includes a first set of application program interfaces 114 and optionally a second set of application program interfaces 116 that the user/patient vital sign results data 108, 110 and 112 is communicated to and from the multi-vital-sign capture system(s) 104 in the device/user layer 102 between one or more hubs 118, bridges 120, interface engines 122 and gateways 124 in the middle layer 106. The middle layer 106 further includes an interoperability device manager component 126 that deploys data such as primary communication protocol, configuration settings, firmware modifications and representations of an authorized location to the multi-vital-sign capture system(s) 104 in the device/user layer 102. The interoperability device manager component 126 sends the data via a 3G, 4G or 5G cellular communication path 128, a WiFi® communication path 130, a Bluetooth® communication path 132 and/or a near-field communication (NFC) path 134. The interoperability device manager component 126 receives the device health data via 3G, 4G or 5G cellular communication path 136 or a WiFi® communication path 138 from the multi-vital-sign capture system(s) 104 in the device/user layer 102.

The one or more hubs 118, bridges 120, interface engines 122 and gateways 124 in the middle layer 106 communicate via a wireless communication path 140 and/or an internet/intranet communication path 142 to an EMR/clinical data repository 144. The EMR/clinical data repository 144 includes an EMR system 146, an electronic health record 148, patient portal medical records 150, a clinical monitoring system 152 and a clinical data repository 154. The wireless communication path 140 can be a 3G, 4G or 5G cellular communication path, or a NFC communication path. The EMR system 146 is located within or controlled by a hospital facility. The electronic health record 148 is a patient file that is managed or controlled by an ambulatory medical facility or a private medical office. One example of Bluetooth® protocol is Bluetooth Core Specification Version 2.1 published by the Bluetooth SIG, Inc. Headquarters, 5209 Lake Washington Blvd NE, Suite 350, Kirkland, Wash. 98033.

FIG. 2 is a block diagram of apparatus of an EMR capture system 200, according to an implementation in which an interoperability manager component manages all communications in the middle layer. In EMR capture system 200, an interoperability manager component 202 manages all communications in the middle layer 106 between the device/user layer 102 and the first set of application program interfaces 114 and the optional second set of application program interfaces 116. In EMR capture system 200, the operation of the device/user layer 102 and the EMR/clinical data repository 144 is the same as in the EMR capture system 100.

FIG. 3 is a block diagram of an overview of an electronic medical records capture system 300, according to an implementation. FIG. 3 shows high level components of the EMR data capture system 300 that includes a bridge 302. The bridge 302 transfers patient measurement records (PMRs) 150 from multi-vital-sign capture system(s) 104 to EMR systems in hospital and clinical environments. Each PMR 150 includes patient measurement data, such as biological vital sign 2136 in FIG. 21-23, estimated body core temperature 2120 in FIG. 21, estimated body core temperature 2212 in FIGS. 21 and 25, biological vital sign 2136 in FIG. 21-23 and 3416 in FIG. 34-37, and heartrate 3910, respiratory rate 3916 and EKG 3930 in FIG. 39. Examples of multi-vital-sign capture system(s) 104 include the multi-vital sign (MVS) system in FIG. 4, the multi-vital-sign capture systems in FIG. 21-23, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000. In some implementations, the multi-vital-sign capture system(s) 104 includes a temperature estimation table that is stored in memory. The temperature estimation table is a lookup table that correlates a sensed forehead temperature to a body core temperature. The correlation of sensed forehead temperature to body core temperature is a significant advance in the technology of the multi-vital-sign capture systems in FIG. 21-23, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000 in FIG. 50, because the correlation has been developed to a highly accurate degree, to an extent of accuracy that surpasses all other multi-vital-sign capture systems, apparatus that estimates a body core temperature, apparatus of variation amplification, hand-held devices, multi-vital-sign capture systems and tablets, that for the first time provides sufficient accuracy to be used in medical clinics.

The EMR data capture system 300 includes two important aspects:

1. A server bridge 302 to control the flow of patient measurement data from multi-vital-sign capture system(s) 104 to one or more and to manage local multi-vital-sign capture system(s) 104.

2. The transfer of patient measurement data in a PMR 150, anonymous, and other patient status information to a cloud based EMR/clinical data repository 144.

The bridge 302 controls and manages the flow of patient measurement data to an EMR/clinical data repository 144 and another EMR/clinical data repository 144 and provides management services to multi-vital-sign capture system(s) 104. The bridge 302 provides an interface to: a wide range of proprietary EMR/clinical data repository 144, location specific services, per hospital, for verification of active operator, and if necessary, patient identifications, and a cloud based EMR/clinical data repository 144) of one or more multi-vital-sign capture system(s) 104, for the purpose of storing all measurement records in an anonymous manner for analysis. A setup, management and reporting mechanism also provided. The bridge 302 accepts communications from multi-vital-sign capture system(s) 104 to: Data format conversion and transferring patient measurement records to EMR/clinical data repository 144, manage the firmware and configuration settings of the multi-vital-sign capture system(s) 104, determine current health and status of the multi-vital-sign capture system(s) 104, support device level protocol for communications, TCP/IP. The support device level protocol supports the following core features: authentication of connected device and bridge 302, transfer of patient measurement records to bridge 302 with acknowledgement and acceptance by the bridge 302 or EMR acceptance, support for dynamic update of configuration information and recovery of health and status of the multi-vital-sign capture system(s) 104, support for firmware update mechanism of firmware of multi-vital-sign capture system(s) 104. The EMR data capture system 300 provides high availability, 24/7/365, with 99.99% availability.

The EMR data capture system 300 provides a scalable server system to meet operational demands in hospital operational environments for one or both of the following deployable cases: 1) A local network 311 at an operational site in which the bridge 302 provides all features and functions in a defined operational network 311 to manage a system of up to 10,000+ multi-vital-sign capture system(s) 104. 2) Remote or cloud based EMR/clinical data repository 144 in which the bridge 302 provides all services to many individual hospital or clinical sites spread over a wide geographical area, for 1,000,000+ multi-vital-sign capture system(s) 104. The EMR capture system also identifies the patient through a unique ID based on the Medical Record Number (MRN) from the hospital or clinical monitoring EMR. This unique ID can be managed through a token based software system in some implementations to allow for compiling time series data on the patient. This data can be used to correlate the effect of medication on vital signs which is useful in clinical trials and patient monitoring. The unique ID is also secure such that if there is a security breach in the EMR capture system the patients MRN number cannot be recovered from the secure token.

The bridge 302 provides a central management system for the multi-vital-sign capture system(s) 104 that provides at least the following functions: 1) configuration management and update of the multi-vital-sign capture system(s) 104 2) device level firmware for all of the multi-vital-sign capture system(s) 104 and 3) management and reporting methods for the multi-vital-sign capture system(s) 104. The management and reporting methods for the multi-vital-sign capture system(s) 104 provides (but not limited to) health and status of the multi-vital-sign capture system(s) 104, battery level, replacement warning of the multi-vital-sign capture system(s) 104, check/calibration nearing warning of the multi-vital-sign capture system(s) 104, rechecking due to rough handling or out of calibration period of the multi-vital-sign capture system(s) 104, history of use, number of measurements, frequency of use etc. of the multi-vital-sign capture system(s) 104, display of current device configuration of the multi-vital-sign capture system(s) 104, Date/time of last device communications with each of the multi-vital-sign capture system(s) 104.

The bridge 302 provides extendable features, via software updates, to allow for the addition of enhanced features without the need for additional hardware component installation at the installation site. The bridge 302 provides a device level commission mechanism and interface for the initial setup, configuration and test of multi-vital-sign capture system(s) 104 on the network 311. The bridge 302 supports multi-vital-sign capture systems that are not hand-held.

Coverage of the EMR data capture system 300 in a hospital can include various locations, wards, ER rooms, offices, physician's Offices etc. or anywhere where automatic management of patient biological vital sign information is required to be saved to a remote EMR system.

The multi-vital-sign capture system(s) 104 can communicate with a third party bridge 312 to provide access to data storage services, EMR systems, multi-vital-sign capture system cloud storage system etc.

Networking setup, configuration, performance characteristics etc. are also determined and carried out by the third party bridge 312 or another third party, for the operational environments. The multi-vital-sign capture system can support the network protocols for communication with the third party bridge 312 devices.

Some implementations of FIG. 3 the bridge 302 is a remote cloud based bridge. The remote cloud based bridge and the EMR/clinical data repositories 144 are operably coupled to the network 311 via the Internet 316.

2. Implementation Details of the Overview Section

In some implementations, a push data model is supported by the EMR data capture system 300 between the multi-vital-sign capture system(s) 104 and the bridge 302 in which connection and data are initially pushed from the multi-vital-sign capture system(s) 104 to the bridge 302. Once a connection has been established and the multi-vital-sign capture system(s) 104 and the bridge 302, such as an authenticated communication channel, then the roles may be reversed where the bridge 302 controls the flow of information between the multi-vital-sign capture system(s) 104 and the EMR/clinical data repository 144.

In some implementations, the multi-vital-sign capture system(s) 104 are connected via a wireless communication path, such as a WiFi® connection to WiFi® access point(s) 304. In other implementations, the multi-vital-sign capture system(s) 104 are connected to a docking station via a wireless or physical wired connection, such as local WiFi®, Bluetooth®, Bluetooth® Low Energy, serial, USB, etc., in which case the docking station then acts as a local pass-through connection and connects to the bridge 302 via a LAN interface and/or cellular or WiFi® link from the docking station to the bridge. In some implementations, the multi-vital-sign capture system(s) 104 are connected via a 3G, 4G or a 5G cellular data communication path to a cellular communication tower 306 which is operably coupled to a cell service provider's cell network which is operably coupled to a bridge/access point/transfer to a LAN or WLAN. In some implementations one or more multi-vital-sign capture system(s) 104 are connected a smartphone 308 via a communication path such as a Bluetooth® communication path, a 3G, 4G or a 5G cellular data communication path, a USB communication path, a WiFi® communication path, or a WiFi® direct communication path to the cell phone; and the smartphone 308 is connected to a cellular communication tower 306 via a 3G, 4G or a 5G cellular data communication path, the cell tower being operably coupled to a cell service provider's cell network which is operably coupled to a bridge/access point/transfer to a LAN or WLAN.

In some implementations, the portable multi-vital-sign capture system(s) 104 includes a battery with limited battery power and lifetime that in some implementations needs to be conserved in order to reduce the intervals at which the battery needs to be recharged. These portable multi-vital-sign capture system(s) 104 support various power saving modes and as such each device is responsible for the initiation of a connection to the wireless network or a wired network and the subsequent connection to the bridge 302 that meets their own specific operational requirements, which provides the multi-vital-sign capture system(s) 104 additional control over their own power management usage and lifetime.

In some implementations in which the multi-vital-sign capture system(s) 104 attempt connection to the bridge 302, the bridge 302 is allocated a static Internet protocol (IP) address to reduce the IP discovery burden on the multi-vital-sign capture system(s) 104 and thus connect the multi-vital-sign capture system to the bridge 302 more quickly. More specifically, the multi-vital-sign capture system(s) 104 are not required to support specific discovery protocols or domain name service (DNS) in order to determine the IP address of the bridge 302. It is therefore important in some implementations that the bridge 302 IP address is static and does not change over the operational lifetime of EMR data capture system 300 on the network 311. In other implementations, a propriety network discovery protocol using UDP or TCP communications methods is implemented. In other implementations, the multi-vital-sign capture system(s) 104 have a HTTP address of a remote sever that acts as a discovery node for the multi-vital-sign capture system(s) 104 to obtain a connection to a remote system or to obtain that remote systems network address.

In some implementations installation of a new multi-vital-sign capture system(s) 104 on the network 311 requires configuration of the multi-vital-sign capture system(s) 104 for the bridge 302 of IP address and other essential network configuration and security information. Commissioning of a multi-vital-sign capture system(s) 104 on the network 311 in some implementations is carried out from a management interface on the bridge 302. In this way a single management tool can be used over all lifecycle phases of a multi-vital-sign capture system(s) 104 on the network 311, such as deployment, operational and decommissioning.

In some implementations the initial network configuration of the multi-vital-sign capture system(s) 104 does not require the multi-vital-sign capture system(s) 104 to support any automated network level configuration protocols, WPS, Zeroconfi etc. Rather the bridge 302 supports a dual network configuration, one for operational use on the operational network of the hospital or clinic, or other location, and an isolated local network, with local DHCP server, for out of the box commissioning of a new multi-vital-sign capture system(s) 104 and for diagnostic test of the multi-vital-sign capture system(s) 104. Multi-vital-sign capture system(s) 104 can be factory configured for known network settings and contain a default server IP address on the commissioning network 311. In addition the multi-vital-sign capture system(s) 104 are required in some implementations to support a protocol based command to reset the multi-vital-sign capture system(s) 104 to network factory defaults for test purposes.

In some situations, the firmware revision(s) of the multi-vital-sign capture system(s) 104 are not consistent between all of the multi-vital-sign capture systems 104 in the operational environment. Therefore the bridge 302 is backwards compatible with all released firmware revisions from firmware and protocol revision, data content and device settings view point of the multi-vital-sign capture system(s) 104. As a result, different revision levels of multi-vital-sign capture system(s) 104 can be supported at the same time on the network 311 by the bridge 302 for all operations.

FIG. 4 is a block diagram of a Multi-Vital Sign (MVS) system 400, according to an implementation. The MVS system 400 includes three communicatively coupled devices; a Multi-Parameter Sensor box (MPSB) 402, a Non-Contact Human Multi-Vital Sign (NCPMVS) device 404 and a multi-vital-sign finger cuff 406. The MVS system 400, the MPSB 402 and the NCPMVS device 404 are all examples of the multi-vital-sign capture system(s) 104. In some implementations, the MVS system 400 captures, stores and exports raw data from all supported sensors in the multi-vital-sign finger cuff 406. MVS system 400 provides a flexible human vital sign measurement methodology that supports different measurement methods and techniques. The MVS system 400 can be used in a clinical setting or a home setting for the collection of human vital signs. The ‘Parameter’ in ‘Multi-Parameter Sensor box’ refers to the vital-signs that are measured by the Multi-Parameter Sensor box 402, such as temperature, heart rate at rest, heart rate variability, respiration, SPO2, blood flow, blood pressure, total hemoglobin (SpHb), PVi, methemoglobin (SpMet), acoustic respiration rate (RRa), carboxyhemoglobin (SpCO), oxygen reserve index (ORi), oxygen content (SpOC), ECG (1 LEAD and 3 LEAD) and/or EEG of a human. The MPSB 402 can be configured to detect blood pressure only, Sp02 only, heart rate only, respiration only, or any combination of vital signs that the MPSB 402 is capable of detecting. The NCPMVS device 404 includes non-slip/slide exterior surface material.

The multi-vital-sign finger cuff 406 and the MPSB 402 are operably coupled to each other through an air line 408 and a communication path 410, such as high speed serial link. A high speed serial link is especially important because the cable of a serial link is quite a bit a bit thinner and more flexible than a parallel cable, which provides a lighter cable that can be more easily wrapped around the MPSB 402. A cuff bladder of the multi-vital-sign finger cuff 406 expands and contracts in response to air pressure from the air line 408.

Some implementations of the multi-vital-sign finger cuff 406 include a finger occlusion cuff 416 and a SPO2 subsystem 418. The multi-vital-sign finger cuff 5400 in FIG. 54-61 is one example of the multi-vital-sign finger cuff 406. The finger occlusion cuff 416 and a SPO2 subsystem 418 are shown in greater detail in FIG. 54-61. In some implementations, the finger occlusion cuff 416 includes at least one miniaturized dynamic light scattering (mDLS) sensor and the SPO2 subsystem 418 includes a photoplethysmogram (PPG) sensor. SPO2 subsystem 5402 in FIG. 54-61 is one example of the SPO2 subsystem 418. SPO2 subsystem 418 and the finger occlusion cuff 416 are operably coupled to a common board in the multi-vital-sign finger cuff 406 and the common board is operably coupled through the communication path 410 to a printed circuit board that is in the base of the MPSB 402.

In some implementations, the multi-vital-sign finger cuff 406 integrates a photoplethysmogram (PPG) sensor and at least one miniaturized dynamic light scattering (mDLS) sensor into a single sensor, both of the which are attached to the multi-vital-sign finger cuff 406. The PPG and mDLS implementation of the multi-vital-sign finger cuff 406 measures the following primary and secondary human vital sign measurements through a PPG sensor from either an index finger or a middle finger; on both the left and right hands at heart height to ensure an accurate measurement: 1) Primary human vital sign measurements such as blood pressure (diastolic and systolic), SPO2, heart rate and respiration rate. 2) Secondary human vital sign measurements include heart rate variability and blood flow. The MPSB 402 can estimate the following vital signs: heart rate at rest, heart rate variability, respiration rate, SPO2 blood oxygenation, blood pressure, total hemoglobin (SpHb), PVi, methemoglobin (SpMet), acoustic respiration rate (RRa), carboxyhemoglobin (SpCO), oxygen reserve index (ORi), oxygen content (SpOC), ECG (1 LEAD and 3 LEAD) and EEG. The heart rate at rest is estimated from data from the PPG sensor. The respiration rate and heart rate variability and the blood pressure diastolic is estimated from data from the mDLS sensor and the PPG sensor. The respiration and the blood pressure systolic is estimated from data from the mDLS sensor. The SPO2 blood oxygenation is estimated from data from the PPG sensor. The PPG sensor optically measures light that passes through tissue from two IR light emitters. The PPG sensor includes one infrared detector that detects infrared energy at two different transmitted wavelength: red and near infrared. Signal fluctuations of the light are generally attributed to the fluctuations of the local blood volume due to the arterial blood pressure wave, which means that the amount of blood in the illuminated perfused tissue fluctuates at the rate of heartbeats. So does the light transmission or light refraction. Therefore, PPG data is an indirect method of the estimation of the blood volume changes. A PPG sensor that measures multiple wavelengths of light is thereby able to determine more than two forms of hemoglobin, including carboxyhemoglobin (SpCO), methemoglobin (SpMet), and total hemoglobin (SpHb). The blood pressure is estimated from data from the mDLS sensor in conjunction with a blood pressure finger cuff which mimics pressure cycle to create an occlusion like the arm cuff. The biological target is illuminated by a laser, the signal is collected by a detector and the time dependency of the laser speckle characteristics are analyzed. The typical mDLS geometry is designed to create direct signal scattering reflection of the signal into the detector. Each mDLS sensor includes two photo diode receivers and one laser transmitter. The advantage of using a finger cuff in conjunction with an SPO2 monitor is the ability to measure patients with low perfusion (e.g. blood oxygenation in the finger). Conventionally, the only method to measure SPO2 in low perfusion patients is to use expensive SPO2 monitors with a large number of sensors. Using the finger occlusion cuff 416, the blood flow can be temporarily increased after occlusion for 10-20 seconds which will allow for an accurate SPO2 measurement. This technique can be used with either reflective of transmission SPO2 sensors.

In some implementations, the multi-vital-sign finger cuff 406 is replaceable, detachable and removable from the MPSB 402. In some implementations, the multi-vital-sign finger cuff 406 is integrated into the MPSB 402. The multi-vital-sign finger cuff 406 that is replaceable, detachable and removable from the MPSB 402 is beneficial in two ways: 1) the cuff assembly is replaceable in the event of damage 2) the cuff assembly can be detached from the MPSB 402 and then attached to a custom connector cable (pneumatic & electrical) that allows a patient to wear the cuff for continuous monitoring, and (3) servicing the device. The replaceable multi-vital-sign finger cuff 406 can have photo optic component(s) (e.g. 2× mDLS and PPG) that are cleanable between patients and replaceable in the event of failure of the inflatable cuff or the photo optic component(s). In some implementations, the cuff bladder of the removable multi-vital-sign finger cuff 406 is translucent or transparent to transparent to the mDLS laser wavelengths and which in some implementations allows the position of the multi-vital-sign finger cuff 406 to be adjusted in relation to specific parts of human anatomy for optimal function of the sensors and comfort to the patient.

The optically measured signal fluctuations measured by PPG are generally ascribed to the fluctuations of the local blood volume due to the arterial blood pressure wave. It means that the amount of blood in the illuminated perfused tissue fluctuates at the rate of heartbeats. So does the light transmission or light refraction. Therefore, PPG is considered as an indirect method of the estimation of the blood volume changes.

A raw PPG signal has a AC pulsation on top of a DC signal component. The pulsation reflects the change of blood volume with each heartbeat. For an optical signal of intensity I₀ and the measured signal is of intensity I, then according to simplified model provides: I=I ₀·exp(−μ*_(d) ·AC(t)·X+(μ_(tissue)+μ_(venous)))

where the most important component is AC(t) associated with arterial blood pulsation. In this model, the optical transmission is governed by the diffusion coefficient of the tissue μ_(tissue) and μ*_(d) of the blood. The last one is dependent on the time dependent parameters: particles concentration c(t) and the particle geometry r(t). The light intensity fluctuation is defined, according to the volumetric model, by the blood thickness changes xb(t). The most general expression assuming that all kind of time dependent processes are involved in the process is: μ*_(d)=(α·μ_(a) ²+β·μ_(a)·μ_(s) ·g)^(1/I(t))

where I(t)≈I₀+(μ_(tissue))·I(μ*_(d) c(t), r(t), x_(b)(t))

where g is the factor of scattering anisotropy and α and β are defined as adjustable parameters:

According to the most simplistic approximations of the diffusion model, the transmission signal behaves as an exponential function of blood thickness xb. Tissue and blood are considered as entirely separate substances. Simply stated, this means the following: In(I(t))=ln(U _(t))−μ_(d)(t)·x _(b)(t)

where Ut is the energy loss due to all non-blood factors.

It is clear that Signal to Noise ration of PPG signal is dependent on AC/DC ratio and on x which is the optical path of the light from the light source to LED's.

The absorption of blood is essentially the absorption of the hemoglobin. The picture below show the absorption spectrum of hemoglobin: It is seen that the strongest absorption is archived for the green light.

In most cases the AC component is only 1% of DC. The information about the pulse is only in AC//component.

Where the reflection geometry is used the light source has to be located distantly from the detector in order to increase the x (depth of penetration). This is because of the optical path must be long enough to enable significant absorption of the light by the blood.

Therefore by nature, the signal of PPG is driven by the multiple scattering effect. Any directly reflected signal (specular reflection) from the surface or glass could violate the multiple scattering assumption resulting in a decrease of AC to DC ratio.

mDLS resembles two technologies: (1) Laser Doppler and (2) Dynamic Light Scattering (DLS). The biological target is illuminated by a laser, the signal is collected by a detector and the time dependency of the laser speckle characteristics are analyzed. The typical mDLS geometry is designed to create direct signal scattering reflection of the signal into the detector.

For the flowing blood, the speckles are created by the relative movement of the red blood cells (shear rate or velocity gradient).

The profile is defined by a type of vessels, blood flow velocity and properties of the blood vessels.

A typical pattern of mDLS signal looks like fluctuations of Intensity.

The analyzed characteristics is the autocorrelation function (ACF) which is calculated from the intensity fluctuations: g2=(I(t)·I(t+τ))/I ²

The mDLS signal includes different components of flowing blood: pulsatile (like in PPG) and non-pulsatile (which does not exist in PPG). Therefore, the ACF can be decomposed to different component of flowing blood and diffusing RBC's by: G(τ)=Σ_(i)ω^(B) _(i) ·gG ^(B) _(i)+Σ_(i)ω^(F) _(i) ·gG ^(F) _(i)

Where index B relates to the Brownian motion and index f relates to the blood flow components. Another way to express the results is by using power spectrum analysis: P(w)=FT(G(τ)) P(t _(c) w)≈∫^(∞) _(−∞) ACF(τ,t _(c))·exp(i,ω,t _(c))·dτ

From this type of the signal processing, both pulsatile and non pusatile components of blood flownamic (e.g. Hemodynamic Indexes (HI)) are obtained. Here are a few examples of HI which are obtained from the one mDLS signal Therefore, the mDLS signal can reveal much more information than PPG, both pusatile and non-pusatile. In addition the mDLS signal can be used for measurement of RBC diffusion which resembles Dynamic Light Scattering Concept (DLS). This information can be used for the assessment of coagulativety and vascular age. Comparison of Pulsatile Component of PPG and mDLS. When pulsatile components of IBP (intravascular blood pressure) are compared, PPG and mDLS the mDLS resembles IBP the most. IBP, PPG, and mDLS have typical blood pulse shapes. The PPG method suffers from low temporal resolution and sensitivity. The mDLS signal provides hemodynamic components which include very specific information about the blood flow associated with different types of vessels. This information is complementary to the pulse and bears an important physiological importance for variety of applications.

The MPSB 402 and the NCPMVS 404 can be operably coupled to each other through a communication path 412 and a 4 point electrical recharge interface (I/F) line 414 to exchange data and control signals. In some implementations, the 4 point electrical recharge interface (I/F) line 414 is a 3 point electrical recharge interface (I/F) line. The MPSB 402 and the NCPMVS 404 do not need to be physically attached to each other for measurement operation by either the MPSB 402 or the NCPMVS 404. In some implementations, the MPSB 402 has at least one universal serial bus (USB) port(s) for bi-directional communication, command, control, status and data transfer with another devices with both standard and propriety protocols using USB infrastructure. USB protocol is defined by the USB Implementers Forum at 5440 SW Westgate Dr. Portland Oreg. 94221. In some implementations, the NCPMVS 404 has at least one USB port(s) for communication with other devices via USB, such as connected to a MPSB 402 for the purposes of transferring the raw sensor data from the device to a computer for analysis.

FIG. 5 is a block diagram of a Multi-Vital Sign (MVS) system 500, according to an implementation. The MVS system 500 includes three communicatively coupled devices; a Multi-Parameter Sensor Box (MPSB) 502, a Non-Contact Human Multi-Vital Sign (NCPMVS) device 503 and a Multi-Parameter Sensor Box Recharge Station (MPSBRS) 504. MPSB 502 is one implementation of MPSB 402 in FIG. 4. NCPMVS 503 is one implementation of NCPMVS 404 in FIG. 4. The MVS system 500, the MPSB 502 and the NCPMVS device 504 are all examples of the multi-vital-sign capture system(s) 104. The NCPMVS 503 captures, stores and exports raw data from all supported sensors in the system. More specifically, the NCPMVS 503 extracts and displays vital sign parameters and transfers the parameters to either a remote third party, hub, bridge etc., or a device manager, or directly to remote EMR/HER/Hospital systems or other third party local or cloud based systems. MVS system 500 provides a flexible human vital sign measurement methodology that supports different measurement methods and techniques. The MVS system 500 can be used in a clinical setting for the collection of human vital signs.

Some implementations of the MPSB 502 include a multi-vital-sign finger cuff 506 that is fixed into the MPSB 502, rather than the replaceable, detachable and removable multi-vital-sign finger cuff 406 in FIG. 4. The multi-vital-sign finger cuff 506 includes a PPG sensor and at least one mDLS sensor. The multi-vital-sign finger cuff 506 is powered via an air line (e.g. 408 in FIG. 4) by a pneumatic engine 507 that provides air pressure to inflate the cuff bladder of the multi-vital-sign finger cuff 506 and the controlled release of that pressure. In some implementations, the air line 408 is ⅙″ (4.2 mm) in diameter. The multi-vital-sign finger cuff 506 in FIG. 5-7 is the same as the mDLS sensors 844 and 846 in FIG. 8, and/or 2142 in FIG. 21-23.

In some implementations, a body surface temperature of a human is also sensed by an infrared finger temperature sensor 508 that is integrated into the MPSB 502 in which the body surface temperature is collected and managed by the MPSB 502. One example of the pneumatic engine 507 is the pneumatic system components 900 in FIG. 9.

In some implementations, a single stage measurement process is required to measure all vital signs in one operation by the NCPMVS 503 by the replaceable, detachable and removable multi-vital-sign finger cuff 406 or the multi-vital-sign finger cuff 506 or the infrared finger temperature sensor 508. However, in some implementations, a two stage measurement process is performed in which the MPSB 502 measures some vital signs through the replaceable, detachable and removable multi-vital-sign finger cuff 406 or the multi-vital-sign finger cuff 506; and in the second stage, the body surface temperature is measured through an infrared temperature sensor 508 in the NCPMVS device 503. One implementation of the infrared finger temperature sensor 508 is digital infrared sensor 2600 in FIG. 26.

The MPSB 502 operates in two primary modes, the modes of operation based on who takes the measurements, a patient or an operator. The two modes are: 1) Operator Mode in which an operator operates the MPSB 502 to take a set of vital sign measurements of another human. The operator is typically clinical staff or a home care giver. 2) Patient Mode in which a patient uses the MPSB 502 to take a set of vital sign measurements of themselves. In some implementations, the MPSB 502 provides both the main measurement modes for patient and operator. The primary measurement areas on the human to be measured are 1) Left hand, index and middle finger, 2) right hand, index and middle finger, and 3) human forehead temperature (requires the other device to perform temperature measurement). The MPSB 502 is portable, light weight, hand held and easy to use in primary and secondary modes of operation in all operational environments.

Given the complex nature of integration into hospital networks, in some implementations, in some implementations the MPSB 502 does not include site communication infrastructure, rather the collected data (vital sign) is extracted from the MPSB 502 via a USB port or by a USB mass storage stick that is inserted into the MPSB 502 or by connecting the MPSB 502 directly to a PC system as a mass storage device itself.

The Non-Contact Human Multi-Vital Sign (NCPMVS) device 503, when connected to a wireless Bluetooth® communication component 513 of the MPSB 502 via a wireless Bluetooth® communication component 514, is a slave to the MPSB 502. The NCPMVS 503 reports status, measurement process, and measurement measurements to the user via the MPSB 502. The NCPMVS 503 provides a user input method to the MPSB 502 via a graphical user interface on a LCD display 515 which displays data representative of the measurement process and status. In one implementation, the wireless Bluetooth® communication component 513 of the MPSB 502 includes communication capability with wireless communication paths (3G, 4G and/or 5G WiFi®, NFC, Z-wave) communication paths and the MPSB 502 is not a slave to the captures vital sign data and transmits the vital sign data via the wireless Bluetooth® communication component 513 in the MPSB 502 to the middle layer 106 in FIG. 1 or the NCPMVS 503 transmits the vital sign data via the communication component 516 of the NCPMVS 503 to the bridge 302, the WiFi® access point 304 in FIG. 3, the cellular communications tower 306, the third party bridge 312 in FIG. 3.

In some implementations, the NCPMVS 503 provides communications with other devices via a communication component 516 of the NCPMVS 503. The communication component 516 has communication capability with cellular communication paths (3G, 4G and/or 5G) and/or WiFi® communication paths. For example, the MPSB 502 captures vital sign data and transmits the vital sign data via the wireless Bluetooth® communication component 513 in the MPSB 502 to the wireless Bluetooth® communication component 514 in the NCPMVS 503, and the NCPMVS 503 transmits the vital sign data via the communication component 516 of the NCPMVS 503 to the middle layer 106 in FIG. 1 or the NCPMVS 503 transmits the vital sign data via the communication component 516 of the NCPMVS 503 to the bridge 302, the WiFi® access point 304 in FIG. 3, the cellular communications tower 306, the third party bridge 312 in FIG. 3. The NCPMVS 503 also includes at least one internal rechargeable battery 517 and user interface keys 518.

In some implementations, when the NCPMVS 503 is connected to the MPSB 502, the NCPMVS 503 performs human bar code scan or identification entry as requested by MPSB 502, the NCPMVS 503 performs an operator bar code scan or identification entry as requested by MPSB 502, the NCPMVS 503 performs human temperature measurement as requested by MPSB 502, the NCPMVS 503 displays information that is related to the MPSB 502 direct action, the NCPMVS 503 starts when the MPSB 502 is started, and the NCPMVS 503 is shutdown under the direction and control of the MPSB 502, and the NCPMVS 503 has a self-test mode that determines the operational state of the MPSB 502 and sub systems, to ensure that the MPSB 502 is functional for the measurement. In other implementations, when the NCPMVS 503 is connected to the MPSB 502, the NCPMVS 503 performs human bar code scan or identification entry as requested by NCPMVS 503, the NCPMVS 503 performs an operator bar code scan or identification entry as requested by NCPMVS 503, the NCPMVS 503 performs human temperature measurement as requested by NCPMVS 503 and the NCPMVS 503 displays information that is related to the MPSB 502 direct action. In some implementations, the information displayed by the NCPMVS 503 includes date/time, human identification number, human name, vitals measurement such as blood pressure (diastolic and systolic), SPO2, heart rate, temperature, respiratory rate, MPSB 502 free memory slots, battery status of the NCPMVS 503, battery status of the MPSB 502, device status of the MPSB 502, errors of the NCPMVS 503, device measurement sequence, measurement quality assessment measurement, mode of operation, subject and operator identification, temperature, measurement, display mode and device revision numbers of the NCPMVS 503 and the MPSB 502. In some implementations, when a body surface temperature of a human is also sensed by an infrared sensor in the Non-Contact Human Multi-Vital Sign (NCPMVS) device 503, the body surface temperature is collected and managed by the MPSB 502. In other implementations, when a body surface temperature of a human is sensed by an infrared sensor in the Non-Contact Human Multi-Vital Sign (NCPMVS) device 503, the body surface temperature is not collected and managed by the MPSB 502.

In some implementations, the Multi-Parameter Sensor Box (MPSB) 502 includes the following sensors and sensor signal capture and processing components that are required to extract the required primary and secondary human vital signs measurements: the multi-vital-sign finger cuff 506 that includes a PPG sensor and two mDLS sensors, the infrared finger temperature sensor 508 and an ambient temperature sensor 512, and in some further implementation, non-disposable sensors for other human measurements. In some implementations, data sample rates for PPG sensor is 2×200 Hz×24 bit=9600 bits/sec, for each of the mDLS sensors is 32 kHz×24 bit=1,572,864 bit/sec and for the ambient temperature sensor is less than 1000 bps. Two mDLS sensors are included in the MPSB 502 to ensure that one or both sensors delivers a good quality signal, thus increasing the probability of obtaining a good signal from a mDLS sensor.

The NCPMVS 503 device performs concurrent two stage measurement processes for all measurements. The measurement process performed by the NCPMVS 503 device is controlled and guided from the NCPMVS 503 device via the GUI on the MPSB 502. The measurements are sequenced and configured to minimize time required to complete all measurements. In some implementations, the NCPMVS 503 device calculates the secondary measurements of heart rate variability and blood flow. The NCPMVS 503 device commands and controls the MPSB 502 via a wireless Bluetooth® protocol communication line 412 and in some further implementations, the MPSB 502 communicates to other devices through Bluetooth® protocol communication line (not shown), in addition to the communications with the NCPMVS 503 device, which could also be concurrent. In some further implementations, the NCPMVS 503 communicates to other devices through Bluetooth® protocol communication line (not shown), in addition to the communications with the MPSB 502 device, which could also be concurrent.

MPSB 502 includes a USB port 519 for interface with the NCPMVS 503 device only, such as the NCPMVS 503, to perform the following functions: recharge the internal rechargeable batteries 520 of the MPSB 502, export sensor data sets to a windows based computer system, firmware update of the MPSB 502 via an application to control and manage the firmware update of the MPSB 502 and configuration update of the MPSB 502. The MPSB 502 does not update the NCPMVS 503 device firmware. The MPSB 502 also includes internal rechargeable batteries 520 that can be recharged via a USB port 522, which provides charge, and the MPSB 502 also includes an external direct DC input providing a fast recharge. The internal batteries of the MPSB 502 can be recharged when the MPSB 502 is powered-off but while connected to USB or DC input. In some implementations, the MPSB 502 can recharge the NCPMVS 503 device from its internal power source over a wireless charging connection. In some implementations, the internal rechargeable batteries 520 provide sufficient operational life of the MPSB 502 on a single charge to perform at least 2 days of full measurements before recharging of the internal rechargeable batteries 520 of the MPSB 502 is required.

In some implementations, the MPSB 502 includes an internal non-volatile, non-user removable, data storage device 524 for up to 20 human raw measurement data sets. The data storage device 524 can be removed by a technician when the data storage device 524 is determined to be faulty. A human measurement set contains all measurement data and measurements acquired by the MPSB 502, including the temperature measurement from the NCPMVS 503. The internal memory is protected against data corruption in the event of an abrupt power loss event. The MPSB 502 and the NCPMVS 503 have a human-form fit function sensor and device industrial/mechanical design. The MPSB 502 also includes anti-microbial exterior material to and an easy clean surface for all sensor and device surfaces. The MPSB 502 stores in the data storage device 524 an “atomic” human record structure that contains the entire data set recording for a single human measurement containing all human raw sensor signals and readings, extracted human vitals, and system status information. The MPSB 502 includes self-test components that determine the operational state of the MPSB 502 and sub systems, to ensure that the MPSB 502 is functional for measurement. The MPSB 502 includes a clock function for date and time. In some implementations. The date and time of the MPSB 502 is be updated from the NCPMVS 503. In some implementations, the MPSB 502 includes user input controls, such as a power on/off switch (start/stop), an emergency stop control to bring the multi-vital-sign finger cuff to a deflated condition. In some implementations, all other input is supported via the NCPMVS 503 via on screen information of the NCPMVS 503. In some implementations, the MPSB 502 includes visual indicators 526 such as a fatal fault indicator that indicates device has failed and will not power up, a device fault indicator (that indicates the MPSB 502 has a fault that would affect the measurement function), battery charging status indicator, battery charged status indicator, a battery fault status indicator.

The components (e.g. 506, 507, 508, 512, 513, 519, 520, 522, 524 and 526) in the MPSB 502 are controlled by a control process and signal processing component 527. The control process and signal processing component 527 can be implemented by a microprocessor or by a FPGA.

The Multi-Parameter Sensor Box Recharge Station (MPSBRS) 504, provides electrical power to recharge the MPSB 502. The MPSBRS 504 can provide electrical power to recharge the batteries of the MPSB 502 either via a physical wired connection or via a wireless charger 530. In some implementations, the MPSBRS 504 does not provide electrical power to the MPSB 502 because the MPSB 502 includes internal rechargeable batteries 520 that can be recharged via either USB port 522 or a DC input. The MPSBRS 504 includes a security lock system 532, a LED status indicator 534, a power supply 536, a main alternating current input 538 and MPSB battery recharge controller 540.

NCPMVS 503 includes a connection status indicator (connected/not connected, fault detected, charging/not charging), a connected power source status indicator, (either USB or DC input) and a power On/Off status indicator. The visual indicators are visible in low light conditions in the home and clinical environment.

The MPSB 502 is hand held and portable, weighing no more than 0.2 Kg. In other implementations, that MPSB 502 has a heavy weight, over 0.5 kg, in order to have mechanical stability on a table. The MPSB 502 includes non-slip/slide exterior surface material.

FIG. 6 is a block diagram of a Multi-Parameter Sensor Box (MPSB) 600, according to an implementation. MPSB 600 is one implementation of MPSB 402 in FIG. 4 and MPSB 600 is one implementation of MPSB 502 in FIG. 5. The MPSB 600 captures, stores and exports raw data from all supported sensors in the system. MPSB 600 supports a variety measurement methods and techniques. The MPSB 600 can be used in a clinical setting for the collection of human vital signs.

A sensor management component 602 controls and receives data from a multi-vital-sign finger cuff 506, a pump, valve, and pressure sensor (shown in FIG. 9) an infrared finger temperature sensor 508, a proximity sensor 604 and another sensor 606. The sensor management component 602 can be implemented in the control process and signal processing component 527 in FIG. 5, which can be implemented by a microprocessor or by a FPGA.

MPSB 600 also includes a CMOS camera 608 that is operably coupled to a USB port 519. The CMOS camera captures images that are processed for reading a barcode to identify the patient and by motion amplification components for determining heart rate, respiratory rate, and blood pressure, a lens 610 is coupled to the CMOS camera 608.

In some implementations, the MPSB 600 can include a 3D camera which is two 2-dimensional cameras separated by a distance. The 3D camera can be used to calculate the depth of objects in different ranges depending on the distance between the two cameras. Motion amplification can be run on both cameras to allow mutual information on heart and respiratory rate. Also, since the accuracy of 3D cameras at 1 [m] can be +/−1 [mm], 3D cameras can provide more accurate respiratory rate measurements. Furthermore 3D camera allow for quantification and characterization of wounds. 3D Cameras can also be used for real-time seizure detection by real-time analysis the frequency of the motion. Seizure motion and high frequency like “twitches” as opposed to a normal more deliberate motion.

The multi-vital-sign finger cuff 506 is integrated into the MPSB 600, rather than the replaceable, detachable and removable multi-vital-sign finger cuff 406 in FIG. 4. The multi-vital-sign finger cuff 506 includes a PPG sensor and at least one mDLS sensor. The multi-vital-sign finger cuff 506 is powered via an air line (e.g. 408 in FIG. 4) by the pneumatic engine 507 that provides air pressure to inflate and deflate the cuff bladder of the multi-vital-sign finger cuff 506 and real time measurement.

In some implementations the PPG sensor in MPSB 600 can be a reflective PPG sensor which measures the reflection of light at two frequencies to determine SPO2. The advantage of a reflective SPO2 sensor is that it is non-touch since the transmitter and receiver can be mounted next to each other.

In some implementations, a body surface temperature of a human is also sensed by the infrared finger temperature sensor 508 that is integrated into the MPSB 600 in which the body surface temperature is collected and managed by the MPSB 600.

In some implementations, a single stage measurement process is required to measure all vital signs in one operation by the MPSB 600 by the replaceable, detachable and removable multi-vital-sign finger cuff 406 or the multi-vital-sign finger cuff 506 or the infrared finger temperature sensor 508. However, in some implementations, a two stage measurement process is performed in which the MPSB 600 measures some vital signs through the replaceable, detachable and removable multi-vital-sign finger cuff 406 or the multi-vital-sign finger cuff 506; and in the second stage, the body surface temperature is measured through an infrared temperature sensor 508 in the NCPMVS device 503.

The MPSB 600 operates in two primary modes, the modes of operation based on who takes the measurements, a patient or an operator. The two modes are: 1) Operator Mode in which an operator operates the MPSB 600 to take a set of vital sign measurements of another human. The operator is typically clinical staff or a home care giver. 2) Patient Mode in which a patient uses the MPSB 600 to take a set of vital sign measurements of themselves. In some implementations, the MPSB 600 provides both the main measurement modes for patient and operator. The primary measurement areas on the human to be measured are 1) face 2) forehead 3) Left hand, index and middle finger and 4) right hand, index and middle finger. The MPSB 600 is portable, light weight, hand held and easy to use in primary and secondary modes of operation in all operational environments.

Given the complex nature of integration into hospital networks, in some implementations, the MPSB 600 does not include site communication infrastructure, rather the collected data (vital sign) is extracted from the MPSB 600 via a USB port or by a USB mass storage stick that is inserted into the MPSB 600 or by connecting the MPSB 600 directly to a PC system as a mass storage device itself.

The Non-Contact Human Multi-Vital Sign (NCPMVS) device 503, when connected to a wireless Bluetooth® communication component 513 of the MPSB 600 via a wireless Bluetooth® communication component 514, is a slave to the MPSB 600. The NCPMVS 503 reports status, measurement process, and measurement measurements to the user via the MPSB 600.

When the NCPMVS 503 is connected to the MPSB 600, the NCPMVS 503 performs patient bar code scan or identification entry as requested by MPSB 600, the NCPMVS 503 performs an operator bar code scan or identification entry as requested by MPSB 600, the NCPMVS 503 performs human temperature measurement as requested by MPSB 600, the NCPMVS 503 displays information that is related to the MPSB 600 direct action, the MPSB 600 starts when the NCPMVS 503 is started, and the MPSB 600 is shutdown under the direction and control of the NCPMVS 503. In some implementations, the information displayed by the NCPMVS 503 includes battery status of the MPSB 600, device status of the MPSB 600, MPSB 600 display mode and device revision numbers of the NCPMVS 503 and the MPSB 600. In some implementations, when a body surface temperature of a human is also sensed by an infrared sensor 508 in the Non-Contact Human Multi-Vital Sign (NCPMVS) device 503, the body surface temperature is collected and managed by the MPSB 600.

In some implementations, the Multi-Parameter Sensor Box (MPSB) 600 includes the following sensors and sensor signal capture and processing components that are required to extract the required primary and secondary human vital signs measurements: the multi-vital-sign finger cuff 506 that includes a PPG sensor and two mDLS sensors, the infrared finger temperature sensor 508, a proximity sensor 604 and another non-disposable sensor(s) for other human measurements sensor 606 or ambient temperature sensor 512. In some implementations, the MBSB 600 can monitor environmental parameters like humidity, air quality pressure in order to understand the environment in which the measurements take place.

The MPSB 600 performs concurrent two stage measurement processes for all measurements. The measurement process performed by the MPSB 600 is controlled and guided from the MPSB 600 via the GUI on the NCPMVS 503 device. The measurements are sequenced and configured to minimize time required to complete all measurements. In some implementations, the MPSB 600 calculates the secondary measurements of heart rate variability and blood flow. The MPSB 600 commands and controls the NCPMVS 503 via a wireless Bluetooth® protocol communication line 412 and in some further implementations, the NCPMVS 503 communicates to the communications with the MPSB 600, which could also be concurrent.

In some implementations, the MPSB 600 includes a USB On-the-Go port 519 for interface with slave devices only, such as the NCPMVS 503, to perform the following functions: recharge the internal rechargeable batteries 520, export sensor data sets to a windows based computer system, firmware update of the MPSB 600 via an application to control and manage the firmware update of the MPSB 600 and configuration update of the MPSB 600. The MPSB 600 does update the NCPMVS 503 device firmware. The internal batteries of the MPSB 600 can be recharged when the MPSB 600 is powered-off but while connected to USB or DC input. In some implementations, the MPSB 600 can recharge the NCPMVS 503 device from its internal power source over a wireless charging connection. In some implementations, the internal rechargeable batteries 520 provide sufficient operational life of the MPSB 600 on a single charge to perform at least 2 days of full measurements before recharging of the internal rechargeable batteries 520 of the MPSB 600 is required. Other common health monitoring devices that can be included with the USB on-the-go port are CO2 monitors, EKG leads. In some implementations, EKG leads and CO2 monitoring equipment can be integrated directly into the finger cuff to optimize cable management and simplify workflow.

In some implementations, the MPSB 600 includes visual indicators 526 such as a fatal fault indicator that indicates the MPSB 600 has failed and will not power up, a device fault indicator (that indicates the MPSB 600 has a fault that would affect the measurement function), a battery charging status indicator, a battery charged status indicator, and/or a battery fault status indicator.

The MPSB 600 also includes a cellular communication module 612 (this could be integrated into the processor) for communications via cell communication frequencies and a WiFi® communication module 614 (this could be integrated into the processor) for communications via WIF communication frequencies. In some implementations, the MPSB 600 also includes an audio sub-system d616 that controls at one or more speakers 618 to enunciate information to an operator or patient via tones, polymorphic and general music/speech capability.

MPSB 600 includes a microprocessor 620 that controls and communicates with the sensor management component 602, the CMOS camera 608, the lens 610, the cellular communication module 612, the WiFi® communication module 614, the audio sub-system 616, speakers 618, the USB port 519, the batteries 520 and the visual indicators 526. In some implementations, the sensor management component 602 is a component of the microprocessor 620.

The MPSB 600 is hand held and portable, weighing no more than 0.2 Kg. In other implementations, the MPSB 600 has a heavy weight, over 0.5 kg, in order to have mechanical stability on a table. The MPSB 600 includes non-slip/slide exterior surface material.

FIG. 7 is a block diagram of a Multi-Parameter Sensor Box (MPSB) 700, according to an implementation. MPSB 700 is one implementation of MPSB 402 in FIG. 4, MPSB 700 is one implementation of MPSB 502 in FIG. 5 and MPSB 700 is one implementation of MPSB 600 in FIG. 6. The MPSB 700 captures, stores and exports raw data from all supported sensors in the system. MPSB 700 supports a variety measurement methods and techniques. The MPSB 700 can be used in a clinical setting for the collection of human vital signs.

A microprocessor 702 controls and receives data from a multi-vital-sign finger cuff 506, a pneumatic engine 507, an infrared finger temperature sensor 508, a proximity sensor 604 and another sensor 606. The sensor management component 602 in FIG. 7 can be implemented in the control process and signal processing component 527 in FIG. 5, which can be implemented by a microprocessor or by a FPGA. In some implementations the microprocessor 702 is an advanced reduced instruction set processor.

The multi-vital-sign finger cuff 506 is integrated into the MPSB 700, rather than the replaceable, detachable and removable multi-vital-sign finger cuff 406 in FIG. 4. The multi-vital-sign finger cuff 506 includes a PPG sensor and at least one mDLS sensor. The multi-vital-sign finger cuff 506 is powered via an air line (e.g. 406 in FIG. 4) by the pneumatic engine 507 that provides air pressure to inflate the cuff bladder of the multi-vital-sign finger cuff 506 and the that provides control signal to deflate the cuff bladder of the multi-vital-sign finger cuff 506.

In some implementations, a body surface temperature of a human is also sensed by the infrared finger temperature sensor 508 that is integrated into the MPSB 700 in which the body surface temperature is collected and managed by the MPSB 700.

In some implementations, a single stage measurement process is required to measure all vital signs in one operation by the MPSB 700 by the replaceable, detachable and removable multi-vital-sign finger cuff 406 or the multi-vital-sign finger cuff 506 or the infrared finger temperature sensor 508. However, in some implementations, a two stage measurement process is performed in which the MPSB 700 measures some vital signs through the replaceable, detachable and removable multi-vital-sign finger cuff 406 or the multi-vital-sign finger cuff 506; and in the second stage, the body surface temperature is measured through an infrared temperature sensor 508 in the NCPMVS device 503.

The Non-Contact Human Multi-Vital Sign (NCPMVS) device 503, when connected to a wireless Bluetooth® communication component 513 of the MPSB 700 via a wireless Bluetooth® communication component 514, is a slave to the MPSB 700. The NCPMVS 503 reports status, measurement process, and measurement measurements to the user via the MPSB 700.

In some implementations, the measurement process performed by the MPSB 700 is controlled and guided from the MPSB 700 via the GUI on the NCPMVS 503 device. The measurements are sequenced and configured to minimize time required to complete all measurements. In some implementations, the MPSB 700 calculates the secondary measurements of heart rate variability and blood flow. The MPSB 700 commands and controls the NCPMVS 503 via a wireless Bluetooth® protocol communication line 412 and in some further implementations, the NCPMVS 503 communicates to the communications with the MPSB 700, which could also be concurrent.

MPSB 700 includes a USB port 519 that is operably coupled to the microprocessor 702 for interface with slave devices only, such as the NCPMVS 503, to perform the following functions: recharge the internal rechargeable batteries 520, export sensor data sets to a windows based computer system, firmware update of the MPSB 700 via an application to control and manage the firmware update of the MPSB 700 and configuration update of the MPSB 700.

In some implementation recharging the internal rechargeable batteries 520 via the USB port 519 is controlled by a battery power management module 710. The battery power management module 710 receives power from a direct connect charging contact(s) 712 and/or a wireless power subsystem 714 that receives power from a RX/TX charging coil 716. The internal rechargeable batteries 520 of the MPSB 700 can be recharged when the MPSB 700 is powered-off but while connected to USB port 519 or DC input via the direct connect charging contacts 712. In some implementations, the MPSB 700 can recharge the NCPMVS 503 device from its internal power source over a wireless charging connection. In some implementations, the internal rechargeable batteries 520 provide sufficient operational life of the MPSB 700 on a single charge to perform at least 2 full days of measurements before recharging of the internal rechargeable batteries 520 of the MPSB 700 is required. In some implementations, system voltage rails 717 are operably coupled to the battery power management module 710.

In some implementations, the MPSB 700 includes an internal non-volatile, non-user removable, data storage device 524 for up to 2 full days of human raw measurement data sets. In some implementations, the MPSB 700 includes a Serial Peripheral Interface (SPI) 704 that is configured to connect to an eternal flash storage system 706.

In some implementations, the MPSB 700 includes a Mobile Industry Processor Interface (MIPI) 708 that is operably connected to the microprocessor 702 and a display screen 709. The microprocessor 702 is also operably coupled to the visual indicators 526.

The MPSB 700 also includes a WiFi® communication module 614 for communications via WiFi® communication frequencies and the MPSB 700 also includes an enterprise security module 718 a cellular communication module 612 for communications via cell phone communication frequencies. The WiFi® communication module 614 and the cellular communication module 612 are operably coupled to an antenna that is located with a case/housing of the MPSB 700.

The MPSB 700 also includes an audio sub-system 616 that controls at one or more speakers 618 to enunciate information to an operator or patient. In some implementations, the microprocessor 702 also controls a haptic motor 722 through the audio sub-system 616. User controls 724 also control the haptic motor 722. A pulse-width modulator 726 that is operably coupled to a general-purpose input/output (GPIO) 728 (that is operably coupled to the microprocessor 702) provides control to the haptic motor 722.

The MPSB 700 is hand held and portable, weighing no more than 0.2 Kg. In other implementations, the MPSB 700 has a heavy weight, over 0.5 kg, in order to have mechanical stability on a table. The MPSB 700 includes non-slip/slide exterior surface material.

In some further implementations the MPSB 600 in FIG. 6 and MPSB 700 in FIG. 7 perform continuous spot monitoring on a predetermined interval with automatic transfer to remote systems via WiFi®, cellular or Bluetooth® communication protocols, with and without the use of a NCPMVS device, and alarm monitoring and integration into clinical or other real time monitoring systems, integration with the sensor box, with the MPSB acting as a hub, for third party sensors, such as ECG, or from direct connect USB or wireless devices, e.g. Bluetooth® patches.

Wireless/network systems (WiFi®, cellular 3G, 4G or 5G) or Bluetooth®) are quite often unreliable. Therefore in some implementations, the NCPMVS devices and the MPSB devices manage vital sign measurements for later transmission.

FIG. 8 is a block diagram of a front end of a multi-vital-sign finger cuff 800, according to an implementation. The front end of a multi-vital-sign finger cuff 800 is one implementation of a portion of a multi-vital-sign finger cuff 406 in FIG. 4. The front end of a multi-vital-sign finger cuff 800 captures, stores and exports raw data from all supported sensors in the system. The front end of a multi-vital-sign finger cuff 800 supports a variety measurement methods and techniques. The front end of a multi-vital-sign finger cuff 800 can be used in a clinical setting for the collection of human vital signs.

The front end of a multi-vital-sign finger cuff 800 includes a front-end sensor electronic interface 802 that is mechanically coupled to a front-end subject physical interface 804. The front-end sensor electronic interface 802 includes a PPG sensor 806 that is electrically coupled to a multiplexer 808 and to a PPG controller 810. The front-end sensor electronic interface 802 includes a mDLS sensor 811 that is electrically coupled to a multiplexer 812 which is coupled to a MDLS controller 813. The front-end sensor electronic interface 802 includes a mDLS sensor 814 that is electrically coupled to a multiplexer 816 and mDLS controller 817. The front-end sensor electronic interface 802 includes an ambient temperature sensor 512. The front-end sensor electronic interface 802 includes a 3-axis accelerometer 818.

The PPG controller 810 is electrically coupled to a controller 820 through a Serial Peripheral Interface (SPI) 822. The mDLS controller 813 is electrically coupled to the controller 820 through a SPI 824. The mDLS sensor 814 is electrically coupled to the controller 820 through a SPI 826. The ambient temperature sensor 512 is electrically coupled to the controller 820 through a I2C interface 828. The 3-axis accelerometer 818 is electrically coupled to the controller 820 through the I2C interface 828.

Visual indicator(s) 526 are electrically coupled to the controller 820 through a general-purpose input/output (GPIO) interface 830. A serial port 832 and a high speed serial port 834 are electrically coupled to the controller 820 and a serial power interface 836 is electrically coupled to the high speed serial port 834. A voltage regulator 838 is electrically coupled to the controller 820. A sensor front-end test component is electrically coupled to the controller 820 through the GPIO interface 830.

A PPG sensor cover 848 is mechanically coupled to the PPG sensor 806, a finger pressure cuff 850 is mechanically coupled to the front-end subject physical interface 804 and a pneumatic connector 852 is mechanically coupled to the finger pressure cuff 850.

FIG. 9 is a block diagram of a pneumatic system components 900, according to an implementation. The pneumatic system components 900 is one component of the multi-vital-sign finger cuff 406 in FIG. 4 and/or the multi-vital-sign finger cuff 506 in FIG. 5. The pneumatic system components 900 are in the MPSB 402, 502, 600, 700 and the front end of a multi-vital-sign finger cuff 800.

The pneumatic system components 900 includes an inflatable cuff bladder 902. The inflatable cuff bladder 902 is one implementation of the finger pressure cuff 850 in FIG. 8. The inflatable cuff bladder 902 is mechanically coupled to a pneumatic pump 904 that provides air pressure to inflate the inflatable cuff bladder 902. The inflatable cuff bladder 902 is mechanically coupled to the pneumatic pump 904 via an air line 906, such as air line 408. The pneumatic pump 904 is one implementation of the pneumatic engine 507. The inflatable cuff bladder 902 is mechanically coupled to a pressure sensor 908 that measures pneumatic pressure in the inflatable cuff bladder 902. The air line 906 is mechanically coupled to a valve 910 that controls pressure from the pneumatic pump 904 to the inflatable cuff bladder 902.

FIG. 10 is a block diagram of a Multi-Vital Sign (MVS) system 1000, according to an implementation. The MVS system 1000 includes two communicatively coupled devices; a Multi-Parameter Sensor Box (MPSB) 502 and a Non-Contact Human Multi-Vital Sign (NCPMVS) device 503. NCPMVS 503 is one implementation of NCPMVS 503 in FIG. 5. A multi-vital-sign finger cuff 506, pneumatic engine 507, an air line 408 and an infrared finger temperature sensor 508 are integrated into the MPSB 502. The MVS system 1000 captures, stores and exports raw data from all supported sensors in the MVS system 1000. MVS system 1000 provides a flexible human vital sign measurement methodology that supports different measurement methods and techniques. The MVS system 1000 can be used in a clinical setting for the collection of human vital signs.

FIG. 11 is a block diagram of a Multi-Vital Sign (MVS) system 1000, according to an implementation. In FIG. 11, the NCPMVS 503 is physically inserted into the MPSB 502. The MVS system 1100 includes three communicatively coupled devices; a Multi-Parameter Sensor Box (MPSB) 402, a multi-vital-sign finger cuff 406 and a Non-Contact Human Multi-Vital Sign (NCPMVS) device 404. MPSB 402 is one implementation of MPSB 402 in FIG. 4. NCPMVS 404 is one implementation of NCPMVS 404 in FIG. 4. The multi-vital-sign finger cuff 406 is replaceable, detachable and removable from the MPSB 402 in comparison to a multi-vital-sign finger cuff 506 of FIG. 5 that is integrated into the MPSB 402. The MVS system 1200 captures, stores and exports raw data from all supported sensors in the system. MVS system 1100 provides a flexible human vital sign measurement methodology that supports different measurement methods and techniques. The MVS system 1100 can be used in a clinical setting for the collection of human vital signs.

FIG. 12 is a block diagram of a Multi-Vital Sign (MVS) system 1200, according to an implementation. In FIG. 12, the NCPMVS 503 is physically inserted into the MPSB 502.

FIG. 13 is a block diagram of a Multi-Vital Sign (MVS) system 1200, according to an implementation. In FIG. 13, the NCPMVS 404 is physically inserted into the MPSB 402. FIG. 14 is a data flow diagram 1400 of the Non-Contact Human Multi-Vital Sign (NCPMVS) device 503, according to an implementation. Data flow diagram 1400 is a process of the MPSB 502 via a graphical user interface on a LCD display 515 on the NCPMVS device 503.

In data flow diagram 1400, a main screen 1402 is displayed by the NCPMVS device 503 that provides options to exit the application 1404, display configuration settings 1406, display data export settings 1408 or display patient identification entry screen 1410. The configuration settings display 1406 provides options for the configuration/management of the NCPMVS device 503. In some implementations, the data flow diagram 1400 includes low power operation and sleep, along startup, initialization, self check and measurement capability of the NCPMVS device 503. The display of data export settings 1408 provides options to take individual measurement of a given vital sign. After the patient identification entry screen 1410 or and alternatively, bar code scanning of both operator and subject, has been completed, one or more sensors are placed on the patient 1412, the NCPMVS device 503 verifies 1414 that signal quality from the sensors is at or above a predetermined minimum threshold. If the verification 1414 fails 1416 as shown in FIG. 15, then the process resumes where one or more sensors are placed on the patient 1412. If the verification 1414 succeeds 1418 as shown in FIG. 16, then measurement 1420 using the one or more sensors is performed and thereafter the results of the measurements are displayed 1422 as shown in FIG. 17 and thereafter the results of the measurements are saved to EMR or clinical cloud 1424, and then the process continues at the main screen 1402. The “para n done” actions the measurement 1420 are indications that the sensing of the required parameters is complete.

FIG. 15 is a display screen 1500 of the Non-Contact Human Multi-Vital Sign (NCPMVS) device 503 indicating that signal quality from the sensors is below a predetermined minimum threshold, according to an implementation.

FIG. 16 is a display screen 1600 of the Non-Contact Human Multi-Vital Sign (NCPMVS) device 503 indicating that signal quality from the sensors is at or above a predetermined minimum threshold, according to an implementation.

FIG. 17 is a display screen 1700 of the Non-Contact Human Multi-Vital Sign (NCPMVS) device 503 showing results of successful multi-vital sign measurements, according to an implementation. The display screen 1700 includes display of the level of WiFi® connectivity 1702 or the level of Bluetooth® connectivity or the level of cellular connectivity, the current time 1704, battery charge level 1706, the patient name 1708 of the patient whose vital signs are measured, measured blood pressure 1710 (systolic and diastolic in terms of millimeters of mercury) of the patient, measured core temperature 1712, measured heartrate in beats per minute 1714, measured SPO2 levels 1716 in the patient bloodstream and measured respiratory rate 1718 in terms of breaths per minute of the patient.

FIG. 18 is a block diagram of an apparatus 1800 to estimate a body core temperature from a forehead temperature sensed by an infrared sensor, according to an implementation. Apparatus 1800 includes a power-initializer 1802 for the infrared sensor 1804 and a time delay 1806 that delays subsequent processing for a period of time specified by the time delay 1806 after power initialization of the infrared sensor 1804 by the power-initializer 1802, such as a delay of a minimum of 340 ms (+20 ms) to a maximum of 360 ms.

Apparatus 1800 includes a voltage level measurer 1808 of the infrared sensor 1804 that outputs a representation of the sensor voltage level 1810 of the infrared sensor 1804. When the sensor voltage level 1810 is below 2.7V or is above 3.5V, a reading error message 1812 is generated and displayed.

Apparatus 1800 also includes a sensor controller 1814 that initiates four infrared measurements 1816 of the forehead surface by the infrared sensor 1804 and receives the four infrared measurements 1816. In some implementations, each of the four infrared measurements 1816 of the forehead surface are performed by the infrared sensor 1804 with a period of at least 135 ms (+20 ms) to a maximum of 155 ms between each of the infrared measurements 1816.

If one of the up to 15 infrared measurements 1816 of the forehead surface by the infrared sensor 1804 that is received is invalid, a reading error message 1812 is displayed.

Apparatus 1800 also includes an ambient temperature controller 1818 that initiates an ambient temperature (Ta) measurement 1820 and receives the ambient temperature (Ta) measurement 1820. If the ambient temperature (Ta) measurement 1820 of the ambient temperature is invalid, a reading error message 1812 is displayed. The ambient temperature controller 1818 compares the ambient temperature (Ta) measurement 1820 to a range of acceptable values, such as the numerical range of 283.15K (10° C.) to 313.15° K (40° C.). If the ambient temperature (Ta) measurement 1820 is outside of this range, a reading error message 1812 is displayed. The sensor controller 1814 compares all four of the infrared measurements 1816 of the forehead surface by the infrared sensor 1804 to determine whether or not are all four are within 1 Kelvin degree of each other. If all four infrared measurements of the forehead surface by the infrared sensor 1804 are not within 1 Kelvin degree of each other, a reading error message 1812 is displayed.

The sensor controller 1814 averages the four infrared measurements of the forehead surface to provide a received object temperature (Tobj) 1822 when all four infrared measurements of the forehead surface by the infrared sensor 1804 are within 1 degree Kelvin of each other. The sensor controller 1814 also generates a voltage-corrected ambient temperature (COvTa) 1824 and a voltage-corrected object temperature (COvTobj) 1826 by applying a sensor voltage correction 1828 to the ambient temperature (Ta) and the object temperature (Tobj) 1822, respectively. For example, the sensor voltage correction 1828 in Kelvin=object temperature (Tobj)−(voltage at sensor−3.00)*0.65. In some implementations, a sensor calibration offset is applied to the voltage-corrected object temperature (COvTobj), resulting in a calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830. For example, a sensor calibration offset of 0.60 Kelvin is added to each voltage-corrected object temperature (COvTobj) from the infrared sensor 1804 of a particular manufacturer.

An estimated body core temperature generator 1832 reads an estimated body core temperature 1834 from one or more tables 1836 that are stored in a memory 1838 (such as memory 1838 in FIG. 18) that correlates the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) to the body core temperature in reference to the voltage-corrected ambient temperature (COvTa) 1824. One implementation of the estimated body core temperature generator 1832 in FIG. 18 is apparatus 1900 in FIG. 19. The tables 1836 are also known as body core temperature correlation tables.

A scale converter 1840 converts the estimated body core temperature 1834 from Kelvin to ° C. or ° F., resulting in a converted body core temperature 1842. There is a specific algorithm for pediatrics (<=8 years old) to account for the different physiological response of children in the febrile>101 deg F range.

FIG. 19-20 are block diagrams of an apparatus 1900 to derive an estimated body core temperature from one or more tables that are stored in a memory that correlate a calibration-corrected voltage-corrected object temperature to the body core temperature in reference to the corrected ambient temperature, according to an implementation. Apparatus 1900 is one implementation of the estimated body core temperature generator 1832 in FIG. 18.

Apparatus 1900 includes an ambient temperature operating-range comparator 1902 that is configured to compare the voltage-corrected ambient temperature (COvTa) (1824 in FIG. 18) to an operational temperature range of the apparatus to determine whether or not the voltage-corrected ambient temperature (COvTa) 1824 is outside of the operational temperature range of the apparatus. The operational temperature range is from the lowest operational temperature of the apparatus 1900 to the highest operational temperature of the MVS system 400. The ambient temperature operating-range comparator 1902 performs block 3222 in FIG. 32. In one example, the operational temperature range is 10.0° C. to 40.0° C.

In a further example, if the voltage-corrected ambient temperature (COvTa) is 282.15° K (9.0° C.), which is less than the exemplary lowest operational temperature (10.0° C.), then the voltage-corrected ambient temperature (COvTa) is outside of the operational temperature range.

Apparatus 1900 includes an ambient temperature table-range comparator 1904 that determines whether or not the voltage-corrected ambient temperature (COvTa) 1824 is outside of the range of the tables. The ambient temperature table-range comparator 1904 performs action 3304 in FIG. 33. For example, if the voltage-corrected ambient temperature (COvTa) is 287.15°×K (14.0° C.), which is less than the lowest ambient temperature the tables, then the voltage-corrected ambient temperature (COvTa) is outside of the range of the tables. In another example, if the voltage-corrected ambient temperature (COvTa) is 312.25° K (39.1° C.), which is greater than the highest ambient temperature (37.9° C.) of all of the tables, then the voltage-corrected ambient temperature (COvTa) is outside of the range of the tables.

When the ambient temperature table-range comparator 1904 determines that the voltage-corrected ambient temperature (COvTa) 1824 is outside of the range of the tables, then control passes to an ambient temperature range-bottom comparator 1906 that is configured to compare the voltage-corrected ambient temperature (COvTa) (1824 in FIG. 18) to the bottom of the range of the tables to determine whether or not the voltage-corrected ambient temperature (COvTa) 1824 is less than the range of the tables. The bottom of the range of the tables is the lowest ambient temperature of all of the tables, such as 14.6° C. Ambient temperature range-bottom comparator 1906 performs block 3306 in FIG. 33. In a further example, if the voltage-corrected ambient temperature (COvTa) is 287.15° K (14.0° C.), which is less than the lowest ambient temperature (14.6° C.) of the tables, then the voltage-corrected ambient temperature (COvTa) is less than the bottom of the range of the tables.

When the ambient temperature range-bottom comparator 1906 determines that the voltage-corrected ambient temperature (COvTa) 1824 is less than the range of the tables, control passes to an estimated body core temperature calculator for hypo ambient temperatures 1908 sets the estimated body core temperature 1834 to the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830+0.19° K for each degree that the voltage-corrected ambient temperature (COvTa) is below the lowest ambient body core table. The estimated body core temperature calculator for hypo ambient temperatures 1908 performs block 3308 in FIG. 33.

For example, when the voltage-corrected ambient temperature (COvTa) is 12.6° C., which is less than the range of the tables, 14.6° C., and the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830 is 29° C. (302.15° K) then the estimated body core temperature calculator for hypo ambient temperatures 1908 sets the estimated body core temperature 1834 to 302.15° K+(0.19° K*(14.6° C.−12.6° C.)), which is 302.53° K.

When the ambient temperature range-bottom comparator 1906 determines that the voltage-corrected ambient temperature (COvTa) 1824 is not less than the range of the tables, control passes to an estimated body core temperature calculator 1910 for hyper ambient temperatures that sets the estimated body core temperature 1834 to the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830—0.13° K for each degree that the voltage-corrected ambient temperature (COvTa) is above the highest ambient body core table. The estimated body core temperature calculator 1910 for hyper ambient temperatures performs block 3310 in FIG. 33.

For example, when the voltage-corrected ambient temperature (COvTa) is 45.9° C., which is above the range of all of the tables, (43.9° C.), and the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830 is 29° C. (302.15° K) then the estimated body core temperature calculator 1910 for hyper ambient temperatures sets the estimated body core temperature 1834 to 302.15° K−(0.13° K*(45.9° C.−43.9° C.)), which is 301.89° K.

When the ambient temperature table-range comparator 1904 determines that the voltage-corrected ambient temperature (COvTa) 1824 is not outside of the range of the tables, then control passes to an ambient temperature table comparator 1912 that determines whether or not the voltage-corrected ambient temperature (COvTa) is exactly equal to the ambient temperature of one of the tables, when the estimated body core temperature calculator 1910 for hyper ambient temperatures determines that the voltage-corrected ambient temperature (COvTa) is within of the range of the tables. The ambient temperature table comparator 1912 performs block 32312 in FIG. 33. When the ambient temperature table comparator 1912 determines that the voltage-corrected ambient temperature (COvTa) is exactly equal to the ambient temperature of one of the tables, then the estimated body core temperature table value selector for exact ambient temperatures 1914 sets the estimated body core temperature 1834 to the body core temperature of that one table, indexed by the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830.

For example, when the voltage-corrected ambient temperature (COvTa) is 34.4° C. (the ambient temperature of Table D) and the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830 is 29.1° C., then the estimated body core temperature table value selector for exact ambient temperatures 1914 sets the estimated body core temperature 1834 to 29.85 C, which is the body core temperature of Table D indexed at the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830 of 29.1° C.

Apparatus 1900 includes a table interpolation selector 1916. When the ambient temperature table comparator 3312 determines that the voltage-corrected ambient temperature (COvTa) is not exactly equal to the ambient temperature of one of the tables, then the table interpolation selector 1916 identifies the two tables which the voltage-corrected ambient temperature (COvTa) falls between. The table interpolation selector 1916 performs block 3318 in FIG. 33.

For example, if the voltage-corrected ambient temperature (COvTa) is 293.25° K (20.1° C.), this ambient value falls between the tables for ambient temperatures of 19.6° C. and 24.6° C., in which case, the 19.6° C. table is selected as the Lower Body Core Table and the 24.6° C. table is selected as the Higher Body Core Table.

Thereafter, apparatus 1900 includes a table interpolation weight calculator 1920 that calculates a weighting between the lower table and the higher table, the table interpolation weights 1922. The table interpolation weight calculator 1920 performs block 3318 in FIG. 33.

For example, when Tamb_bc_low (the voltage-corrected ambient temperature (COvTa) for the Lower Body Core Table)=19.6° C. and T amb_bc_high (the voltage-corrected ambient temperature (COvTa) for the Higher Body Core Table)=24.6 C, then the amb_diff=(Tamb_bc_high−Tamb_bc_low/100)=(24.6−19.6)/100=0.050° C. Further, the Higher Table Weighting=100/((Tamb−Tamb_bc_low)/amb_diff)=100/((20.1−19.6)/0.050)=10% and the Lower Table Weighting=100−Higher Table Weighting=100−10=90%.

Apparatus 1900 includes a body core temperature reader 1924 that reads the core body core temperature that is associated with the sensed forehead temperature from each of the two tables, the Lower Body Core Table and the Higher Body Core Table. The body core temperature reader 1924 performs block 3320 in FIG. 33. The calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830 is used as the index into the two tables.

Apparatus 1900 also includes a correction value calculator 1926 that calculates a correction value 1928 for each of the Lower Body Core Table and the Higher Body Core Table. For example, where each of the tables has an entry of calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830 for each 0.1° Kelvin, to calculate to a resolution of 0.01° Kelvin, the linear difference is applied to the two table values that the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830 falls between.

For example, when the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830 is 309.03° K, then the calibration-corrected voltage-corrected object temperature (COcaCOvTobj) 1830 falls between 309.00 and 309.10. The correction value 1928 is equal to a+((b−a)*0.03), where a=body core correction value for 309.0° K and b=body curve correction value for 309.1° K.

Thereafter, apparatus 1900 includes an estimated body core temperature calculator for interpolated tables 1930 that determines the body core temperature of the sensed forehead temperature in reference to the ambient temperature by summing the weighted body core temperatures from the two tables. The estimated body core temperature calculator for interpolated tables 1930 performs block 3322 in FIG. 33. The estimated body core temperature is determined to equal (Tcor_low*Lower Table Weighting/100)+(Tcor_high*Higher Table Weighting/100).

For example, when the voltage-corrected ambient temperature (COvTa) is 293.25° K (20.10° C.), then in this case 90% (90/100) of the Table) and 10% (10/100) are summed to set the estimated body core temperature 1834.

The comparators (1902, 1904 and 1906) can be arranged in any order relative to each other.

Implementation Alternatives

Operational Features and Implementation Capability

Some implementations of the EMR data capture systems 100, 200 and 300 have limited operational features and implementation capability. A significant function of the EMR data capture systems 100, 200 and 300 with the limited operational features and implementation capability in the bridge 302 is to accept data from a multi-vital-sign capture system(s) 104 and update the EMR/Clinical Data Repository 144. The EMR/Clinical Data Repository 144 can be one or more of the following: Electronic Medical Records System (EMR) 146, Electronic Health Record System (148), Patient Portal Medical Records 150, Clinical Monitoring System 152, and Clinical Data Repository 154.

The following limited feature set in some implementations is supported by the EMR data capture systems 100, 200 and 300 for the demonstrations:

Implementation to a local IT network on a server of the local IT network, OR located on a remote-hosted network, whichever meets the operational requirements for healthcare system.

Acceptance of patient medical records from a multi-vital-sign capture system(s) 104:

a. Date and Time

b. Operator identification

c. Patient identification

d. Vital Sign measurement(s)

e. Device manufacturer, model number and firmware revision

Acceptance of limited status information from a multi-vital-sign capture system(s) 104:

a. Battery Level

b. Hospital reference

c. location reference

d. Manufacturer identification, serial number and firmware revision

e. Unique identification number

Transfer of patient records from a multi-vital-sign capture system(s) 104 to a third party EMR capture system and to the EMR data capture systems 100, 200 and 300, respectively in that order.

User interface for status review of known multi-vital-sign capture system(s) 104.

Configuration update control for active devices providing configuration of:

a. Hospital reference

b. Unit location reference

Limited Operational Features and Implementation Capability

The following features are supported limited operational capability:

A Patient Record Information and measurement display interface for use without submission of that data to an EMR/Clinical Data Repository 144.

Update of device firmware over the wireless network.

Operational Use

Local Network Based—Single Client

In some implementations, the multi-vital-sign capture system(s) 104 are deployed to a local hospital, or other location, wireless IT network that supports WiFi® enabled devices. The multi-vital-sign capture system(s) 104 supports all local network policy's including any local security policy/protocols, such as WEP, WPA, WPA2, WPA-EPA as part of the connection process for joining the network. In some implementations, the multi-vital-sign capture system(s) 104 operates on both physical and virtual wireless LAN's, WAN's, and the multi-vital-sign capture system(s) 104 are configured for operation on a specific segment of the network. Depending on the IT network structure, when the multi-vital-sign capture system(s) 104 is configured for operation on a specific segment of the network, the multi-vital-sign capture system(s) 104 network connection ability is limited to the areas of the operational environment for which it as be configured. Therefore, the multi-vital-sign capture system(s) 104 in network environments that have different network configurations are configured to ensure that when the multi-vital-sign capture system(s) 104 are used in various locations throughout the environment that the multi-vital-sign capture system(s) 104 has access in all required areas.

In some implementations the bridge 302 system is located on the same IT network and deployed in accordance with all local IT requirements and policy's and that the multi-vital-sign capture system(s) 104 on this network are able to determine a routable path to the bridge 302. The multi-vital-sign capture system(s) 104 and the server are not required to implement any network name discovery protocols and therefore the bridge 302 is required to be allocated static IP address on the network. In the case where a secondary bridge device is deployed to the network as a backup for the primary, or the bridge 302 supports a dual networking interface capability, then the secondary bridge IP address is also required to be allocated a static IP address.

A benefit of this bridge 302 implementation to the local IT network infrastructure is the reduction in latency times for data sent between the multi-vital-sign capture system(s) 104 and the bridge 302.

It is important to note that this is a single organization implementation and as such the bridge 302 is configured to meet the security and access requirements of a single organization.

FIG. 3 is a block diagram of an overview of an electronic medical records (EMR) capture system 300 having a remote cloud based bridge 302, according to an implementation.

An implementation of a remote cloud-based bridge 302 for a single client is similar to the local network case described at the end of the description of FIG. 3, with the exception that the bridge 302 may not be physically located at the physical site of the multi-vital-sign capture system(s) 104.

The multi-vital-sign capture system(s) 104 include a temperature estimation table (not shown in FIG. 3). The temperature estimation table is stored in memory. The temperature estimation table is a lookup table that correlates a sensed surface temperature to a body core temperature.

The physical locale of the bridge 302 is transparent to the multi-vital-sign capture system(s) 104.

Again as in the local install case, the same user access and security policies are in place for the single operating organization.

Remote Based—Multiple Client Support

In some implementations for smaller organizations or for organizations that do not have a supporting IT infrastructure or capability that a remote bridge 302 system is deployed to support more than one organization. Where the bridge 302 is deployed to support more than one organization, the bridge 302 can be hosted as a cloud based system. In this case the multi-vital-sign capture system(s) 104 are located at the operational site for the supported different geographical location organizations and tied to the bridge 302 via standard networking methods via either private or public infrastructure, or a combination thereof.

Where a remote, i.e. non-local IT network, system is deployed to support more than one hospital or other organization EMR data capture systems 100, 200 and 300 includes components that isolate each of the supported organizations security and user access policy's and methods along with isolating all data transfers and supporting each organizations data privacy requirements. In addition system performance is required to be balanced evenly across all organizations. In this case each organization can require their specific EMR data capture systems 100, 200 and 300 be used and their EMR data capture systems 100, 200 and 300 are concurrently operational with many diverse EMR/Clinical Repository systems such as Electronic Medical Record System EMR 146, Electronic Health Record 148, Patient Portal Medical Records 150, Clinical Monitoring System 152, and Clinical Data Repository 154.

Single Measurement Update

The primary function of the multi-vital-sign capture system(s) 104 is to take vital sign measurements, for example, a patient body core temperature, display the result to the operator and to save the patient information and body core temperature to an EMR/Clinical Data Repository 144.

Normally the multi-vital-sign capture system(s) 104 are in a low power state simply waiting for an operator to activate the unit for a patient measurement. Once activated by the operator EMR data capture systems 100, 200 and 300 will power up and under normal operating conditions guide the operator through the process of patient body core temperature measurement and transmission of the patient record to the bridge 302 for saving using the EMR data capture systems 100, 200 and 300.

Confirmation at each stage of the process to the operator is required, to ensure a valid and identified patient result is obtained and saved to the EMR, the key last confirmation point is: Saving of data to the bridge 302.

In some implementations, the confirmation at each stage in some implementations is provided by the operator through either the bridge 302, multi-vital sign capture system(s) 104, or the EMR/Clinical Data Repository 144.

When confirmation is provided by the bridge 302 it is an acknowledgment to the multi-vital-sign capture system(s) 104 that the bridge 302 has accepted the information for transfer to the EMR/Clinical Data Repository 144 in a timely manner and is now responsible for the correct management and transfer of that data.

When confirmation is provided by the EMR, the bridge 302 is one of the mechanisms via which the confirmation is returned to the multi-vital-sign capture system(s) 104. That is the multi-vital-sign capture system(s) 104 sends the data to the bridge 302 and then waits for the bridge 302 to send the data to the EMR and for the EMR to respond to the bridge 302 and then the bridge 302 to the multi-vital-sign capture system(s) 104.

In some implementations depending on the operational network and where the bridge 302 is physically located, i.e. local or remote, that the type of confirmation is configurable.

In some implementations, the multi-vital-sign capture system(s) 104 maintains an internal non-volatile storage mechanism for unsaved patient records if any or all of these conditions occur: The multi-vital-sign capture system(s) 104 cannot join the network. The multi-vital-sign capture system(s) 104 cannot communicate with the bridge 302. The multi-vital-sign capture system(s) 104 does not receive level confirmation from either the bridge 302 or the EMR/Clinical Data Repository 144. The multi-vital-sign capture system(s) 104 must maintain the internal non-volatile storage mechanism in order to fulfill its primary technical purpose in case of possible operational issues. When the multi-vital-sign capture system(s) 104 has saved records present in internal memory of the multi-vital-sign capture system(s) 104, then the multi-vital-sign capture system(s) 104 attempts to transfer the saved records to the bridge 302 for processing in a timely automatic manner.

Periodic Connectivity

The multi-vital-sign capture system(s) 104 in order to obtain date/time, configuration setting, provides status information to the bridge 302, transfers saved patient records and checks for a firmware update to provide a mechanism on a configured interval automatically that powers up and communicates to the configured bridge 302 without operator intervention.

Accordingly and outside of the normal clinical use activation for the multi-vital-sign capture system(s) 104, the multi-vital-sign capture system(s) 104 can both update its internal settings, and provide status information to the bridge 302 system.

If these actions were left to the operator, startup case of the multi-vital-sign capture system(s) 104 for operational clinical use then there may be an unacceptable delay to the operator in proceeding to the measurement action of the multi-vital-sign capture system(s) 104.

Automatic Transfer of Saved Patient Measurement Records (PMRs)

If the multi-vital-sign capture system(s) 104 for an unknown reason has been unable to either join the network or connect to the bridge 302 or receive a bridge 302 or EMR data level acknowledge that data has been saved the multi-vital-sign capture system(s) 104 allows the primary clinical body core temperature measurement function to be performed and saves the resultant PMR in non-volatile internal memory up to a supported, configured, maximum number of saved patient records on the multi-vital-sign capture system(s) 104.

When the multi-vital-sign capture system(s) 104 are started for a measurement action the multi-vital-sign capture system(s) 104 determines if the multi-vital-sign capture system(s) 104 contains any saved patient records in its internal memory. If one or more saved patient records are detected then the multi-vital-sign capture system(s) 104 attempts to join the network immediately, connect to the bridge 302 and send the patient records one at a time to the bridge 302 device while waiting for the required confirmation that the bridge 302 has accepted the patient record. Note in this case confirmation from the EMR is not required. On receipt of the required validation response from the remote system the multi-vital-sign capture system(s) 104 deletes the patient record from its internal memory. Any saved patient record that is not confirmed as being accepted by the remote device is maintained in the multi-vital-sign capture system(s) 104 internal memory for a transfer attempt on the next power up of the multi-vital-sign capture system(s) 104.

The multi-vital-sign capture system(s) 104 on a configured interval will also carry out this function. In some implementations the multi-vital-sign capture system(s) 104 reduces the interval when saved patient records are present on the multi-vital-sign capture system(s) 104 in order to ensure that the records are transferred to the bridge 302, and subsequently the EMR/Clinical Data Repository 144, in a timely manner once the issue has been resolved. When this transfer mechanism is active status information is presented to the operator on the multi-vital-sign capture system(s) 104 screen.

Under this operation it is possible for the bridge 302 device to receive from a single multi-vital-sign capture system(s) 104 multiple patient record transfer requests in rapid sequence.

Device Configuration

The multi-vital-sign capture system(s) 104 upon 1) connection to the bridge 302, 2) configured interval or 3) operator initiation, transmits to the bridge 302 with the model number and all appropriate revisions numbers and unique identification of the multi-vital-sign capture system(s) 104 to allow the bridge 302 to determine the multi-vital-sign capture system(s) 104 capabilities and specific configurations for that multi-vital-sign capture system(s) 104.

The bridge 302 acts as the central repository for device configuration, either for a single device, a group of defined devices or an entire model range in which the multi-vital-sign capture system(s) 104 queries the bridge 302 for the device parameters of the multi-vital-sign capture system(s) 104 and if the queried device parameters are different from the multi-vital-sign capture system(s) 104, the multi-vital-sign capture system(s) 104 updates the current setting to the new setting values as provided by the bridge 302.

Device Date/Time Update

In implementations where there is no mechanism on the multi-vital-sign capture system(s) 104 for the user to configure date and time on the multi-vital-sign capture system(s) 104 via its user interface.

The real time clock of the multi-vital-sign capture system(s) 104 may drift with time. Therefore each multi-vital-sign capture system(s) 104 connected to the bridge 302 will query the bridge 302 for the current date and time and update the multi-vital-sign capture system(s) 104 internal clock based on the current date and time provided by the bridge 302.

In some implementations, the multi-vital-sign capture system(s) 104 query the bridge 302 on the defined interval or when the multi-vital-sign capture system(s) 104 are started by the operator upon joining the network. Therefore the bridge supports an accurate date and time mechanism, with leap year capability, as per the local IT policy. If no local IT policy is in place then the bridge 302 maintains date and time against a known accurate source, e.g. a web based time server.

Accordingly, in some implementations all devices are maintained at the same date and time across the operation of EMR data capture systems 100, 200 and 300 and the capabilities of the multi-vital-sign capture system(s) 104.

Device Status Management

In some implementations the bridge 302 provides a level of device management for the multi-vital-sign capture system(s) 104 being used with EMR data capture systems 100, 200 and 300. In some implementations, the bridge 302 is able to report and determine at least the following:

Group and sort devices by manufacture, device model, revisions information and display devices serial numbers, unique device identification, asset number, revisions, etc. and any other localized identification information configured into the multi-vital-sign capture system(s) 104, e.g. ward location reference or Hospital reference.

The last time a specific unit connected to EMR data capture systems 100, 200 and 300.

The current status of the given device, battery level, last error, last date of re-calibration of check, or any other health indicator supported by the multi-vital-sign capture system(s) 104.

Report devices out of their calibration period, or approaching their calibration check.

Report devices that require their internal battery replaced.

Report devices that require re-checking due to a detected device failure or error condition, or that have been treated in a harsh manner or dropped.

Determine if a multi-vital-sign capture system(s) 104 has not connected for a period of time and identify the multi-vital-sign capture system(s) 104 as lost or stolen. If the multi-vital-sign capture system(s) 104 reconnects to the network after this period of time then the multi-vital-sign capture system(s) 104 in some implementations is highlighted as requiring an accuracy check to ensure that it is operational. In some implementations, the multi-vital-sign capture system(s) 104 also supports this capability and after a pre-determined time disconnects from the network to inhibit the measurement function of the multi-vital-sign capture system(s) 104 until a multi-vital-sign capture system(s) 104 level recheck is carried out.

Provide a mechanism to commission and decommission devices onto and off of the network. If a multi-vital-sign capture system(s) 104 has not been specifically commissioned for operation on the network then it in some implementations is not be allowed to access the core services supported by the bridge 302 even if it has configured for operation on the EMR data capture systems 100, 200 and 300.

Firmware Update

In some implementations a firmware update for a given device model is scheduled on the network as opposed to simply occurring. When a multi-vital-sign capture system(s) 104 is activated for a patient measurement firmware updates are blocked because the update process delays the patient biological vital sign measurement. Instead the bridge 302 system includes a firmware update roll out mechanism where the date and time of the update can be scheduled and the number of devices being updated concurrently can be controlled.

In some implementations, when a multi-vital-sign capture system(s) 104 connects to the bridge 302 due to a heartbeat event that the multi-vital-sign capture system(s) 104 queries the bridge 302 to determine if a firmware update for that model of device is available and verify if its firmware, via revision number, is required to be updated. The bridge 302 responds to the query by the multi-vital-sign capture system(s) 104 based on whether or not a firmware update is available and the defined schedule for the update process. If an update is available at the bridge 302 but the current time and date is not valid for the schedule then the bridge 302 transmits a message to the multi-vital-sign capture system(s) 104 that there is an update but that the update process is delayed and update the multi-vital-sign capture system(s) 104 firmware check interval configuration. The firmware check interval setting will then be used by the multi-vital-sign capture system(s) 104 to reconnect to the bridge 302 on a faster interval than the heartbeat interval in order to facilitate a more rapid update. For e.g. the firmware update schedule on the bridge 302 in some implementations is set to every night between 2 am and 4 am and the interval timer in some implementations is set to for example, every 15 minutes.

In some implementations the bridge 302 manages the firmware update process for many different multi-vital-sign capture systems 104 each with their specific update procedure, file formats, and verification methods and from a date and time scheduling mechanism and the number of devices being update concurrently. In addition in some implementations the bridge 302 will provide a mechanism to manage and validate the firmware update files maintained on the bridge 302 for use with the multi-vital-sign capture system(s) 104.

This section concludes with short notes below on a number of different aspects of the EMR data capture systems 100, 200 and 300 follow on numerous topics:

Remote—single client operation: The bridge 302 architecture provide remote operation on a hospital network system. Remote operation is seen as external to the network infrastructure that the multi-vital-sign capture system(s) 104 are operational on but considered to be still on the organizations network architecture. This can be the case where a multiple hospital—single organization group has deployed EMR data capture systems 100, 200 and 300 but one bridge 302 device services all hospital locations and the bridge 302 is located at one of the hospital sites or their IT center.

Remote—multiple client operation: The bridge 302 architecture in some implementations is limited to remote operation on a cloud based server that supports full functionality for more than one individual separate client concurrently when a cloud based single or multiple server system is deployed to service one or more individual hospital/clinical organizations.

Multiple concurrent EMR support: For a single remote bridge 302 servicing multiple clients EMR data capture systems 100, 200 and 300 supports connectivity to an independent EMR, and a different EMR vendor, concurrently for each support client. With one bridge 302 servicing multiple clients in some implementations, each client requires the configuration to send data securely to different EMR/Clinical Data Repositories.

Support Different EMR for same client: The bridge 302 architecture for operation in a single client organization supports the user by the organization of different EMR/Clinical Data Repository 144 from different departments of wards in the operational environment. It is not uncommon for a single organization to support multiple different EMR/Clinical Data Repository 144 for different operational environments, for example, Cardiology and ER. EMR data capture systems 100, 200 and 300 in some implementations takes this into account and routes the patient data to the correct EMR/Clinical Data Repository 144. Therefore the bridge 302 is informed for a given multi-vital-sign capture system(s) 104 which indicates to the EMR the medical data has to be routed to.

Segregation of operations for multiple client operations on a single bridge 302:

EMR data capture systems 100, 200 and 300 supports per client interfaces and functionality to ensure that each client's configurations, performance, user accounts, security, privacy and data protection are maintained. For single server implementations that service multiple independent hospital groups the bridge 302 in some implementations maintain all functionality, and performance per client separately and ensure that separate user accounts, bridge 302 configuration, device operation, patient and non-patient data, interfaces etc. are handled and isolated per client. A multiple cloud based implementation obviates this function as each client includes their own cloud based system.

Multiple organization device support: The bridge 302 supports at least 1 million+ multi-vital-sign capture system(s) 104 for a remote implementations that services multiple separate hospital systems. The supported multi-vital-sign capture system(s) 104 can be multi-vital-sign capture system(s) 104 from different manufacturers.

EMR capture system support: The multi-vital-sign capture system(s) 104 supports a wide range of implementations of the EMR data capture system(s) 300 and is capable of interfacing to any commercially deployed EMR/Clinical Data Repository 144.

EMR capture system interface and approvals: The bridge 302 device provides support for all required communication, encryption, security protocols and data formats to support the transfer of PMR information in accordance with all required operational, standards and approval bodies for EMR/Clinical Data Repository 144 supported by the EMR data capture systems 100, 200 and 300.

Remote EMR capture system(s): The bridge 302 supports interfacing to the required EMR/Clinical Data Repository 144 independent of the EMR data capture system(s) 300 location, either locally on the same network infrastructure or external to the network that the bridge 302 is resided on or a combination of both. The EMR data capture systems 100, 200 and 300, or systems, that the bridge 302 is required to interact with and save the patient to can not be located on the same network or bridge 302 implementation location, therefore the bridge 302 implementation in some implementations ensure that the route to the EMR exists, and is reliable.

Bridge buffering of device patient records: The bridge 302 device provides a mechanism to buffer received PMRs from connected multi-vital-sign capture system(s) 104 in the event of a communications failure to the EMR/Clinical Data Repository 144, and when communications has been reestablished subsequently transfer the buffered measurement records to the EMR. From time to time in normal operation, the network connection from the bridge 302 is lost. If communications has been lost to the configured EMR data capture system(s) 300 then the bridge 302 in some implementations accepts measurement records from the multi-vital-sign capture system(s) 104 and buffers the measurement records until communications has be reestablished. Buffering the measurement records allows the medical facility to transfer the current data of the medical facility to the bridge 302 for secure subsequent processing. In this event the bridge 302 will respond to the multi-vital-sign capture system(s) 104 that either 1. Dynamic validation of EMR acceptance is not possible, or 2. The bridge 302 has accepted the data correctly.

Bridge 302 real time acknowledge of EMR save to device: The bridge 302 provides a mechanism to pass to the multi-vital-sign capture system(s) 104 confirmation that the EMR has accepted and saved the PMR. The bridge 302 when configured to provide the multi-vital-sign capture system(s) 104 with real time confirmation that the EMR/Clinical Data Repository 144 (s) have accepted and validated the PMR. This is a configuration option supported by the bridge 302.

Bridge 302 real time acknowledgement of acceptance of device PMR: The bridge 302 provides a mechanism to pass to the multi-vital-sign capture system(s) 104 confirmation that the bridge 302 has accepted the PMR for subsequent processing to the EMR. The multi-vital-sign capture system(s) 104 in some implementations verifies that the bridge 302 has accepted the PMR and informs the operator of the multi-vital-sign capture system(s) 104 that the data is secure. This level of confirmation to the multi-vital-sign capture system(s) 104 is considered the minimum level acceptable for use by the EMR data capture systems 100, 200 and 300. Real time acknowledgement by the bridge 302 of acceptance of the PMR from the device is a configuration option supported by the bridge 302.

Bridge Date and Time: The bridge 302 maintains internal date and time against the local network time source or a source recommended by the IT staff for the network. All transitions and logging events in some implementations are time stamped in the logs of the bridge 302. The multi-vital-sign capture system(s) 104 will query the bridge 302 for the current date and time to update its internal RTC. The internal time of multi-vital-sign capture system(s) 104 can be maintained to a +/−1 second accuracy level, although there is no requirement to maintain time on the multi-vital-sign capture system(s) 104 to sub one-second intervals.

Graphical User Interface: The bridge 302 device provides a graphical user interface to present system information to the operator, or operators of EMR data capture systems 100, 200 and 300. The user interface presented to the user for interaction with EMR data capture systems 100, 200 and 300 in some implementations can be graphical in nature and use modem user interface practices, controls and methods that are common use on other systems of this type. Command line or shell interfaces are not acceptable for operator use though can be provided for use by system admin staff.

Logging and log management: The bridge 302 is required to provide a logging capability that logs all actions carried out on the bridge 302 and provides a user interface to manage the logging information. Standard logging facilities are acceptable for this function for all server and user actions. Advanced logging of all device communications and data transfers in some implementations is also provided, that can be enabled/disable per multi-vital-sign capture system or for product range of multi-vital-sign capture system.

User Accounts: The bridge 302 device provides a mechanism to support user accounts on the multi-vital-sign capture system(s) 104 for access control purposes. Standard methods for user access control are acceptable that complies with the operational requirements for the install/implementation site.

User Access Control: The bridge 302 device supports multiple user access control that defines the access control privileges for each type of user. Multiple accounts of each supported account type are to be support. Access to EMR data capture systems 100, 200 and 300 in some implementations be controlled at a functional level, In some implementations, the following levels of access is provided:

System Admin: provides access to all features and functions of EMR data capture systems 100, 200 and 300, server and device based.

Device Admin: provides access only to all device related features and functions supported by the EMR data capture systems 100, 200 and 300.

Device Operator: provides access only to device usage.

Device Installer: provides access only to device commissioning and test capabilities.

A user account can be configured for permissions for one or more account types.

Multi-User Support: The bridge 302 device is required to provide concurrent multi-user support for access and management of the bridge 302 system across all functions. Providing multiple user access is deemed a necessary operational feature to support.

Modify User Accounts: The bridge 302 provides a method to create, delete, and edit the supported user accounts and supported access privileges per account.

Bridge Data Corruption/Recovery: The bridge 302 architecture and implementation in some implementations ensure that under an catastrophic failure of EMR data capture systems 100, 200 and 300 or a storage component that no data is lost that has not been confirmed as saved to the either the EMR for PMRs or localize storage for operational data pertaining to the non-patient data maintained by the EMR data capture systems 100, 200 and 300. The bridge 302 supports a method to ensure zero data lost under critical and catastrophic system failure of the bridge 302 or any of the bridge 302 components, network interfaces, storage systems, memory contents, etc. for any data handled by the EMR data capture systems 100, 200 and 300. In the event of a recovery action where a catastrophic failure has occurred EMR data capture systems 100, 200 and 300 supports both the recovery action and its normal operational activities to ensure that EMR data capture systems 100, 200 and 300 is active for clinical use.

Bridge availability: The bridge 302 device is a high availably system for fail safe operation 24/7/365, with 99.99% availability, i.e. “four nines” system. The bridge 302 implementation meets an availability metric of 99.99%, i.e. a “four nines” system because the bridge 302 hardware in some implementations is implemented with a redundant dual server configuration to handle single fault conditions. The bridge 302 has an independent power source or when the installation site has a policy for power loss operation the bridge 302 installation in some implementations complies with the policy requirements.

Bridge Static IP address and port Number: The bridge 302 provides a mechanism to configure the bridge 302 for a primary use static IP address and port number. For multi-vital-sign capture system(s) 104 connection to the bridge 302, the bridge 302 in some implementations has a static IP address and that IP address in some implementations is known by the multi-vital-sign capture system(s) 104.

Bridge Dual network capability: The bridge 302 system provides a mechanism to support a dual operational network interface to allow for failure of the primary network interface. This secondary network interface supports a configurable static IP address and port number. A redundant network connection in some implementations is provided to cover the event that the primary network interface has failed. Note if the bridge 302 implementation for EMR data capture systems 100, 200 and 300 employs two separate bridges 302 or other redundant mechanism to provide a backup system then this requirement can be relaxed from an operational view point, however EMR data capture systems 100, 200 and 300 in some implementations support this mechanism.

Local WiFi® commissioning network: The bridge 302 provides a mechanism on the local operational network to commission new multi-vital-sign capture system(s) 104 for operational use. EMR data capture systems 100, 200 and 300 supplies a localized isolated network for the use of commissioning new devices onto the operational network. The bridge 302 has a known default IP address on this network and provides a DHCP server for the allocation of IP address to devices on EMR data capture systems 100, 200 and 300. The commissioning of new devices is to be considered a core aspect of the bridge 302 functions. However it is acceptable that a separate non server based application in some implementations will manage the configuration process provided the same user interface is presented to the user and the same device level configuration options are provided. In some implementations, the configuration of a new multi-vital-sign capture system(s) 104 on the network is carried out in two stages: Stage 1: network configuration from the commissioning network to the operational network. Stage 2: Once joined on the operational network specific configuration of the multi-vital-sign capture system(s) 104 for clinical/system function operation.

Remote commissioning of devices: EMR data capture systems 100, 200 and 300 provides a mechanism where the bridge 302 device is not present on the local network for a new device is to be commissioned on the operational network. Even when the bridge 302 is on a cloud server external to the operational site network new devices in some implementations can be commissioned onto the network in the same manner as if the bridge 302 was a local server. This does not preclude the installation of a commission relay server on to the operational network that supports this mechanism.

Device setup: The bridge 302 supports the configuration of a device level network operation and security settings for an existing or new multi-vital-sign capture system(s) 104 on either the commissioning network or the operational network. New devices are configured on the commissioning network. Existing devices on the operational network are also configurable for network and security requirements independent of the network that the multi-vital-sign capture system(s) 104 are currently connected to the bridge 302 provides the required user interface for the configuration of the network operational and security settings by the operator. Once configured, a method of verifying that the multi-vital-sign capture system(s) 104 have been configured correctly but be presented to the operator to prove that the multi-vital-sign capture system(s) 104 are operational. Devices support a network command to reboot and rejoin the network for this verification purpose.

Bridge Configuration: The bridge provides a mechanism to support configuration of all required specific control options of the bridge 302. A method to configure the bridge 302 functions in some implementations is provided for all features where a configuration option enable, disable or a range of parameters are required.

Bridge multi-vital-sign capture system acknowledgement method: The bridge 302 provides a configuration method to control the type of acknowledgement required by the EMR data capture systems 100, 200 and 300, one of: device configuration dependent, EMR level acknowledgment, bridge 302 level acknowledgement. In some implementations, a multi-vital-sign capture system 104 requires from the bridge an acknowledgement that the PMR has been saved by the EMR data capture systems 100, 200 and 300 or accepted for processing by the bridge 302.

EMR Level: Bridge 302 confirms save by EMR data capture systems 100, 200 and 300.

Bridge Level: bridge 302 controlled, accepted for processing by the bridge 302.

Enabled/Disable of firmware updated mechanism: The bridge 302 provides a method to globally enable or disable the supported multi-vital-sign capture system(s) 104 firmware updated feature. A global enable/disable allows the control of the firmware update process.

Server Management: The bridge 302 is required to provide a user interface that provides configuration and performance monitoring of the bridge 302 and platform functions.

System Reporting: The bridge 302 is required to provide a mechanism to provide standard reports to the operator on all capabilities of the bridge 302 system. Standard reporting in some implementations includes selection of report parameter, sorting of report parameters, srinting of reports, export of reports to known formats, WORD, excel, PDF etc., identification of reports, organization name, location, page numbers, name of report etc., date and time of log, generate by user type and extent of provides full reporting for all system features and logs, examples are: List of devices known to EMR data capture systems 100, 200 and 300, with location reference and date and time of last connection Report on the battery status for all known multi-vital-sign capture system(s) 104. Report on any devices that reported an error Report on devices that have expired calibration dates. Report on devices that are approaching their calibration dates.

Demo Patient Interface: The bridge 302 provides a mechanism for demo only purposes where an EMR data capture systems 100, 200 and 300 is not available for interfacing to EMR data capture systems 100, 200 and 300 to allow patient records received from a given device to be viewed and the biological vital sign data presented. For demonstrations of EMR data capture systems 100, 200 and 300 where there is no EMR data capture systems 100, 200 and 300 to connect the bridge 302 the system provides a user interface method to present the data sent to the bridge 302 by the connected multi-vital-sign capture system(s) 104. In some implementations this patient data interface manages and stores multiple patients and multiple record readings per patient and present the information to the operator in an understandable and consistent manner.

Interface to EMR/clinical data repository 144: The bridge 302 device provides an interface to the EMR/clinical data repository 144 for the purpose of storing patient records. Also, anonymous PMRs are stored for the purposes of data analysis as well as provide a mechanism to monitor the operation of the multi-vital-sign capture system(s) 104.

Device PMRs: The bridge 302 in some implementations accepts propriety formatted measurement records from multi-vital-sign capture system(s) 104 connected and configured to communicate with the bridge 302 and translate the received measurement record into a suitable format for transfer to a EMR data capture systems 100, 200 and 300. The bridge 302 is the multi-vital-sign capture system(s) 104 that will take the multi-vital-sign capture system(s) 104 based data and translate that data into a format suitable to pass along to a local or remote EMR/Clinical Data Repository 144 system using the required protocols of that EMR/Clinical Data Repository 144.

Device non patient measurement data: The bridge 302 in some implementations accepts data from connected multi-vital-sign capture system(s) 104 and provides data to a connected device. This is data or setting parameters associated with the multi-vital-sign capture system(s) 104 that in some implementations is managed by the bridge 302, e.g. device configuration settings, firmware images, status information etc.

Device to Bridge 302 interface protocol: The bridge 302 supports a multi-vital-sign capture system(s) 104 to bridge 302 interface protocol, BRIP, for all communications between the multi-vital-sign capture system(s) 104 and the bridge 302 device. Each device supports a single interface protocol, BRIF and individual device or manufacture level protocols can be supported by the bridge 302.

Network communications method: The bridge 302 supports a LAN based interface for processing connection requests and data transfers from remote multi-vital-sign capture system(s) 104. Standard communications methods such as UDP/TCP/IP etc. are supported but the interface is not restricted to this transfer mechanism, the architecture of EMR data capture systems 100, 200 and 300 in some implementations support other transfer methods such as UDP. Where more than one multi-vital-sign capture system(s) 104 type is supported in EMR data capture systems 100, 200 and 300 the bridge 302 supports different transfer mechanism concurrently Multi-vital-sign capture system(s) 104: The bridge 302 in some implementations accept connections and measurement data records from multi-vital-sign capture system(s) 104.

Non-conforming Multi-vital-sign capture system: The bridge 302 in some implementations accepts connections and measurement data records from non-multi-vital-sign capture system(s) 104 multi-vital-sign capture system(s) 104 using device interface protocols specific to a given device or manufacture of a range of device. The EMR data capture systems 100, 200 and 300 support third party multi-vital-sign capture system(s) 104 to provide the same core features and functions as those outlined in this document. In some implementations, a core system supports all multi-vital-sign capture system(s) 104 connected to EMR data capture systems 100, 200 and 300, for the purposes of measurement data, body core temperature, ECG (electroencephalogram), EEG (electroencephalogram), blood pressure, plus other biological vital signs, both single and continuous measurement based, for transfer to the selected EMR/Clinical Data Repository 144, along with per device configuration and status monitoring.

Single Parameter Measurement Data: The bridge 302 in some implementations accept and processes for transfer to the configured EMR/Clinical Data Repository 144, single event measurement data. Single event measurement data is defined as a patient biological vital sign single point measurement such as a patient body core temperature, blood pressure, heart rate or other data that is considered a one-time measurement event for a single measurement parameter. This type of data is generated from a multi-vital-sign capture system(s) 104 that supports a single biological vital sign reading.

Multiple Parameter Measurement Data: The bridge 302 in some implementations accept and process for transfer to the EMR multiple event measurement data. Multiple event measurement data is defined as a patient biological vital sign single point measurement such as a patient body core temperature, blood pressure, heart rate or other parameter that is considered a one-time measurement event for more than one parameter. This type of data is generated from a multi-biological vital sign multi-vital-sign capture system(s) 104.

Continuous Parameter Measurement Data: The bridge 302 in some implementations accept and process for transfer to the EMR single parameter continuous measurement data. Continuous measurement data is defined as a stream of measurement samples representing a time domain signal for a single or multiple biological vital sign parameter.

Unique Multi-vital-sign capture system identification: The bridge 302 supports a unique identifier per multi-vital-sign capture system(s) 104, across all vendors and device types, for the purposes of device identification, reporting and operations. Each multi-vital-sign capture system(s) 104 that is supported by the EMR data capture systems 100, 200 and 300 provides a unique identification based on the manufacture, product type, and serial number or other factors such as the FDA UID. The bridge 302 is required to track, take account of, and report this number in all interactions with the multi-vital-sign capture system(s) 104 and for logging. This device identification can also be used in the authentication process when a multi-vital-sign capture system(s) 104 connects to the bridge 302.

Device connection authentication: The bridge 302 provides a mechanism to authenticate a given multi-vital-sign capture system(s) 104 on connection to ensure that the multi-vital-sign capture system(s) 104 are known and allowed to transfer information to the bridge 302. Access to the bridge 302 functions in some implementations is controlled in order to restrict access to currently allowed devices only. Acceptance of a multi-vital-sign capture system(s) 104 making connection the bridge 302 for 2 main rationales. 1. The multi-vital-sign capture system(s) 104 are known to the bridge 302, and that 2. A management function to control access for a given device, i.e. allow or bar access.

Device date and time update: The bridge 302 device can provide a mechanism to allow a connected multi-vital-sign capture system(s) 104 to update its internal date and time settings against the bridge 302's current date and time. The multi-vital-sign capture system(s) 104 are to update their internal real time clocks on connection to the bridge 302, accordingly, a time reference across all devices used with EMR data capture systems 100, 200 and 300 is obtained from a central source. All embedded systems real time clock functions drift with time, this mechanism will form the basis of both time and date configuration on the multi-vital-sign capture system(s) 104 and dynamic update of time and date for the multi-vital-sign capture system(s) 104 thereby removing the need to set time and date on a given device. An accuracy of +/−1 second is acceptable for maintaining the time on a multi-vital-sign capture system(s) 104. Bridge 302 to device backwards compatibility: The bridge 302 device is required to be backwards compatible with all released versions of multi-vital-sign capture system(s) 104 firmware, interface protocols, and data formats supported by the bridge 302 device from first release of the bridge 302 system. Backwards compatibly of the bridge 302 with all released revisions of multi-vital-sign capture system(s) 104 in some implementations for the normal operation of EMR data capture systems 100, 200 and 300. It cannot be guarantee that all devices of a given product are at the same revision level or that different products from a single manufacture or from different manufactures will support the same interface protocol or other critical component revision.

Last connection of device: The bridge 302 is required maintain a history of the connection dates and times for a given multi-vital-sign capture system(s) 104. This is required from a reporting and logging viewpoint. In some implementations will also be used to determine if a multi-vital-sign capture system(s) 104 are lost/stolen or failed.

Calibration/Checker Monitoring: The bridge 302 is required to track the valid calibration dates for a given device and present to the operator those devices that are out of calibration or approaching calibration. All multi-vital-sign capture system(s) 104 in some implementations be checked for operation and accuracy on a regular bases. EMR data capture systems 100, 200 and 300 can provide the facility to generate a report and high light devices that are either out of calibration and those approaching calibration. The check carried out by the bridge 302 is on the expiry date exposed by the multi-vital-sign capture system(s) 104. The bridge 302 is not required to actually check the multi-vital-sign capture system(s) 104 for calibration, only report if the multi-vital-sign capture system(s) 104 are out of calibration based on the multi-vital-sign capture system(s) 104 expiry date. In some implementations the expiry date is updated at the time of the multi-vital-sign capture system(s) 104 recalibration check.

Error/Issue monitoring: The bridge 302 is required to track the issues/errors reported by a given device and present that information to the operator in terms of a system report. Reporting of device level errors dynamically for a given device is diagnostics tool for system management. Providing the issue/error history for a given device provides core system diagnostic information for the multi-vital-sign capture system(s) 104.

Battery Life monitoring: The bridge 302 is required to track the battery level of a given device and report the battery level information to the operator. EMR data capture systems 100, 200 and 300 is to highlight to the operator that a given device has an expired or nearly expired or failed internal battery based on the information exposed by the multi-vital-sign capture system(s) 104. It is the multi-vital-sign capture system(s) 104 responsibility to determine its own internal power source charge level or battery condition. The bridge 302 can provide a mechanism to report the known battery condition for all devices, e.g. say all devices that have 10% battery level remaining.

Lost/Stolen/Failed monitoring: The bridge 302 is required to determine for a given multi-vital-sign capture system(s) 104 if it has been lost/stolen/or failed and disable the multi-vital-sign capture system(s) 104 for system operation. Being able to determine if a system has not connected to the bridge 302 for a period of time is a feature for failed, lost or stolen reporting to the operator. If a multi-vital-sign capture system(s) 104 has not connected to EMR data capture systems 100, 200 and 300 for a period of time, EMR data capture systems 100, 200 and 300 determines that the multi-vital-sign capture system(s) 104 has been stolen or lost, in this event the operator is informed in terms of a system report and the multi-vital-sign capture system(s) 104 removed from the supported devices list. If and when the multi-vital-sign capture system(s) 104 reconnects to EMR data capture systems 100, 200 and 300 the multi-vital-sign capture system(s) 104 are to be lighted as “detected” and forced to be rechecked and re-commissioned again for use on the network.

Device Keep Alive: The bridge 302 provides a mechanism to inform a target multi-vital-sign capture system(s) 104 upon connection to the bridge 302 to stay connected to the bridge 302 until released by the bridge 302. A multi-vital-sign capture system(s) 104 keep alive method in some implementations is provided so that the bridge 302 when a multi-vital-sign capture system(s) 104 connects can inform the multi-vital-sign capture system(s) 104 to stay powered and connected to the bridge 302 for the purposes of reconfiguration, status monitoring or diagnostics.

Reset device to network default: A method to reset a target device or group of selected devices to factory settings for all network parameters in some implementations.

Reset device to factory default: A method to reset a target device or group of selected devices to their factory default settings in some implementations is supported.

Dynamic Device Parameter Configuration: The bridge 302 provides a mechanism to provide configuration information to a multi-vital-sign capture system(s) 104 when requested by the multi-vital-sign capture system(s) 104 on connection to the bridge 302 or via the keep device alive mechanism. Upon connecting to a bridge 302 a multi-vital-sign capture system(s) 104 as part of the communications protocol determines if its current configuration is out of date, if any aspect of the multi-vital-sign capture system(s) 104 configuration is out of date and is required to be updated then the bridge 302 provides the current configuration information for the multi-vital-sign capture system(s) 104 model and revision. This is intended to be as simple as the multi-vital-sign capture system(s) 104 getting the configuration setting for each of its supported parameters. The bridge 302 is responsible to ensure that the supplied information is correct for the multi-vital-sign capture system(s) 104 model and revision level.

Device Configuration Grouping: Single device: The bridge 302 provides a mechanism to configure a single device, based on unique device id, to known configuration parameters. The bridge 302 in some implementations allows a single multi-vital-sign capture system(s) 104 to be updated when it connects to the bridge 302 either via the heart beat method or via operator use. This effectively means that the bridge 302 provides a method to manage and maintain individual device configuration settings and have those settings available dynamically for when the multi-vital-sign capture system(s) 104 connects. Further the bridge 302 supports per device configurations for different revisions of device firmware, for example revision 1 of device A has configuration parameters x, y and z, but revision 2 of the multi-vital-sign capture system(s) 104 has configuration parameters has x, y, z and k and the valid allowed range for the y parameter has been reduced.

Device Configuration Grouping—Multi-vital-sign capture system(s) 104 model group: The bridge 302 provides a mechanism to configure all devices within a model range to known configuration parameters. The facility to reconfigure a selected sub-group of devices that are model x and at revision level all with the same configuration information.

Device Configuration Grouping—selected group within model range: The bridge 302 provides a mechanism to configure a selected number of devices within the same model range to known configuration parameters. The facility to reconfigure a selected sub-group of devices that are model x and at revision level y Device Configuration Grouping—defined sub group: The bridge 302 provides a mechanism to configure a selected number of devices with the same model based on device characteristics e.g. revision level, operational location etc. The facility to reconfigure all devices that are model x and at revision level y, OR all model x devices that are in operation in Ward 6 is a feature.

Device Configuration files: The bridge 302 provides a method to save, load, update and edit a configuration file for a multi-vital-sign capture system(s) 104 model number and/or group settings. The ability to save and load configuration files and change the configuration content in the file is a required feature for EMR data capture systems 100, 200 and 300. A file management mechanism in some implementations is also provided for the saved configuration files.

Dynamic configuration content: The bridge 302 in some implementations dynamically per multi-vital-sign capture system(s) 104 connection determine upon request by the multi-vital-sign capture system(s) 104 the new configuration settings for that device, given that the medical devices connect in a random manner to the bridge 302, the bridge 302 is required for the connected device, model, revision, unique identification etc. to maintain the configuration settings for that device.

Association of multi-vital-sign capture system(s) 104 to target EMR/Clinical Data Repository 144. The bridge 302 provides a mechanism to control the patient record received from a multi-vital-sign capture system(s) 104 to transfer the record to one or more of the supported EMR/Clinical Data Repository 144. Where more than one EMR/Clinical Data Repository 144 is maintained by a single organization, e.g. one for ER, cardiology use and possibility one for outpatients etc. EMR data capture systems 100, 200 and 300 in some implementations manage either by specific device configuration or bridge 302 configuration which EMR the patient record is to be transmitted to by the bridge 302.

Device Configuration and Status Display: In some implementations, when a multi-vital-sign capture system(s) 104 connects to the bridge 302 that the multi-vital-sign capture system(s) 104 queries its current configuration settings against the bridge 302 settings for that specific device type and device as outlined below: 1. A given device based on a unique id for that device. Note each device is required to be uniquely identified in EMR data capture systems 100, 200 and 300. 2. A group of devices allocated to a physical location in the hospital, i.e. Based on a ward number of other unique location reference. Accordingly, in some implementations a group of devices in a given location in some implementations is updated separately from other devices of the same type located in a different location in the same hospital environment, i.e. a recovery ward 1 as opposed to an emergency room. A group of devices based on product type, i.e. all multi-vital-sign capture system(s) 104, updated with the same settings. Bridge 302 device configuration options adjusted based on multi-vital-sign capture system(s) 104. The bridge 302 in some implementations adjusts the configuration options presented to the operator based on the capabilities of the multi-vital-sign capture system(s) 104 being configured. Where multiple different multi-vital-sign capture system(s) 104 are supported by the EMR data capture systems 100, 200 and 300 it cannot be assumed that each device from a different manufacture or from the same manufacture but a different model of the same device level configuration parameters. Therefore the bridge 302 in some implementations determine the configuration capabilities for the multi-vital-sign capture system(s) 104 to be configured and present only valid configuration options for that device with valid parameter ranges for these options.

Device parameter Validation: The bridge 302 provides a mechanism for a given model of multi-vital-sign capture system(s) 104 to validate that a given configuration parameter is set within valid parameter ranges for that device model and revision. The bridge 302 is required based on the multi-vital-sign capture system(s) 104 model and revision level to present valid parameter ranges for the operator to configure a multi-vital-sign capture system(s) 104 level parameter with. Device patient record acceptance check response source. The bridge 302 provides a mechanism to configure the multi-vital-sign capture system(s) 104 to require either: 1) a confirmation from the bridge 302 device only that a patient record has been received for processing or 2) a confirmation from the bridge 302 device that the EMR data capture systems 100, 200 and 300 has received and saved the patient information. In some implementations of the configuration of the multi-vital-sign capture system(s) 104 the multi-vital-sign capture system(s) 104 reports to the operator a status indicator.

Device Hospital/Clinic Reference: A device setting to allow an organization identifier to be configured on the multi-vital-sign capture system(s) 104. The multi-vital-sign capture system(s) 104 can be configured with an alphanumeric identification string, max 30 characters that allows the organization to indicate to the hospital/clinic that the multi-vital-sign capture system(s) 104 are in use with, e.g. “Boston General”.

Device Ward Location reference: A device setting to allow an operational location identifier to be configured on the multi-vital-sign capture system(s) 104. The multi-vital-sign capture system(s) 104 are to be configured with an alphanumeric identification string, max 30 characters that allows the organization to indicate an operational area within the organization, e.g. “General Ward #5”.

Device Asset Number: A device setting to allow an organization asset number to be configured on the multi-vital-sign capture system(s) 104. The multi-vital-sign capture system(s) 104 are to be configured with an alphanumeric identification string, max 30 characters to allow the organization to provide an asset tag for the multi-vital-sign capture system(s) 104.

Display device Manufacture Name, Device Model and Serial Number: A method to display the manufacture name, device model number and device serial number for the unit is provided. EMR data capture systems 100, 200 and 300 can provide a method to determine the manufacturer name, model number and device level serial number of for the multi-vital-sign capture system 10. Alphanumeric identification string, max 60 characters in length for each of the three parameters.

Display multi-vital-sign capture system(s) 104 unique identification reference tag: A method to display the device level unique identifier for the unit. For regulatory traceability reasons each device is to support a unique identification number this number in some implementations be displayed by the EMR data capture systems 100, 200 and 300. In some implementations, an alphanumeric identification string is a maximum of 120 characters. This parameter is not to be updateable by the EMR data capture systems 100, 200 and 300.

Device last Check/Calibration Date: A method to display and set the date of the last check or re-calibration action for the multi-vital-sign capture system(s) 104. This allows the bridge 302 to determine which devices are required to be re-checked and present that information to the operator of EMR data capture systems 100, 200 and 300. All multi-vital-sign capture system(s) 104 with a measurement function are required to be checked for accuracy on a regular basis. EMR data capture systems 100, 200 and 300 provides a mechanism to update the multi-vital-sign capture system(s) 104 date of last check/calibration when a device level check has been carried out.

Device Temperature Display units: Configuration option for the displayed body core temperature units for the multi-vital-sign capture system(s) 104, Centigrade or Fahrenheit. For detection of patient body core temperature, the unit in some implementations is configured for reporting body core temperatures in degrees centigrade or Fahrenheit. Default is: Fahrenheit. The bridge 302 also requires a configuration parameter for the display of any temperature results.

Operator scan enable/disable: The bridge 302 can provide a mechanism to enable or disable the multi-vital-sign capture system(s) 104 level operator identification scan action. The operator identification scan capability is to be configurable on a per device basis so that it can be enabled or disabled. Allow Operator Scan Repeat for more than one patient scan: The bridge 302 can provide a mechanism to enable/disable the multi-vital-sign capture system(s) 104 to take a single operator identification scan and associate that identification with multiple patient measurements. Where the clinical work flow allows for a known number of patient scan(s), or predetermined time frame(s), to be taken by a single operator an enable/disable feature for the multi-vital-sign capture system(s) 104 is provided. Default is: disabled Max number of patient scans per operator scan: The bridge 302 can provide a configuration parameter for controlling the number of patient id scans after an operator identification scan before the operator identification scan has to be taken again by the multi-vital-sign capture system(s) 104. The number of patient scans that are allowed to be taken by the multi-vital-sign capture system(s) 104 and assigned the same operator is set to a default value of 1. The bridge 302 can provide a configuration parameter for controlling the time frame in seconds that a single operator identification scan can be used for multiple patient identification scans. A time limit in seconds ranging from 0 to 1800 seconds can be set to allow a multi-vital-sign capture system(s) 104 to associate a single operator identification with multiple patient records in this time. In some implementations, a parameter of 0 disables the time limit range checking. The default is 0.

3. Multi-Vital-Sign Capture System

FIG. 21 is a block diagram of a multi-vital-sign capture system 2100 that includes a digital infrared sensor, a biological vital sign generator and a temporal variation amplifier, according to an implementation. Multi-vital-sign capture system 2100 is an apparatus to measure body core temperature and other biological vital signs. The multi-vital-sign capture system 2100 is one example of the multi-vital-sign capture system 104 and one example of the Multi-Parameter Sensor Box (MPSB) 502.

The multi-vital-sign capture system 2100 includes a microprocessor 2102. The multi-vital-sign capture system 2100 includes a battery 2104, in some implementations a single button 2106, and a digital infrared sensor 2108 that is operably coupled to the microprocessor 2102. The digital infrared sensor 2108 includes digital ports 2110 that provide only digital readout signal 2111. In some implementations the multi-vital-sign capture system 2100 includes a display device 2114 that is operably coupled to the microprocessor 2102. In some implementations, the display device 2114 is a LCD color display device or a LED color display device, which are easy to read in a dark room, and some pixels in the display device 2114 are activated (remain lit) for about 5 seconds after the single button 2106 is released. After the display has shut off, another body core temperature reading can be taken by the apparatus. The color change of the display device 2114 is to alert the operator of the apparatus of a potential change of body core temperature of the human or animal subject. The body core temperature reported on the display device 2114 can be used for treatment decisions.

The microprocessor 2102 is configured to receive from the digital ports 2110 that provide only digital readout signal 2111. In some implementations, the digital readout signal 2111 is representative of an infrared signal 2116 of a forehead surface temperature that is detected by the digital infrared sensor 2108. In other implementations, the digital readout signal 2111 is representative of an infrared signal 2116 of a surface temperature of a human other than the forehead surface that is detected by the digital infrared sensor 2108. A body core temperature estimator 2118 in the microprocessor 2102 is configured to estimate the body core temperature 2120 from the digital readout signal 2111 that is representative of the infrared signal 2116 of the forehead (or other surface), a representation of an ambient air temperature reading from an ambient air sensor 2122, a representation of a calibration difference from a memory location that stores a calibration difference 2124 and a memory location that stores a representation of a bias 2126 in consideration of a temperature sensing mode. In some implementations, the multi-vital-sign capture system 2100 does not include an analog-to-digital converter 2112 operably coupled between the digital infrared sensor 2108 and the microprocessor 2102. Furthermore, the digital infrared sensor 2108 also does not include analog readout ports 2113. The dashed lines of the A/D converter 2112 and the analog readout ports 2113 indicates absence of the A/D converter 2112 and the analog readout ports 2113 in the multi-vital-sign capture system 2100 and the apparatus 2500. One implementation of the digital infrared sensor 2108 is digital infrared sensor 2600 in FIG. 26.

The multi-vital-sign capture system(s) 104 includes a temperature estimation table 2127 in a memory. The temperature estimation table 2127 is a lookup table that correlates a sensed forehead temperature to an estimated body core temperature 2120. The sensed forehead temperature is derived from the digital readout signal 2111.

The temperature estimation table 2127 is stored in a memory. In FIGS. 21-22 and 25, the temperature estimation table 2127 is shown as a component of the microprocessor 2102. The memory that stores the temperature estimation table 2127 can be separate from the microprocessor 2102 or the memory can be a part of the microprocessor 2102, such as cache on the microprocessor 2102. Examples of the memory include Random Access Memory (RAM) 5006 and flash memory 5008 in FIG. 50. In implementations of the multi-vital-sign capture systems in FIG. 21-23, the apparatus that estimates a body core temperature in FIG. 21-22 and 25, the apparatus of variation amplification in FIG. 34-42, the multi-vital-sign capture system 5000 in which speed of the multi-vital-sign capture systems in FIG. 21-23 and the apparatus that estimate a body core temperature of an external source point in FIGS. 21-22 and 25 is very important, storing the temperature estimation table 2127 in memory that is a part of the microprocessor 2102, such as cache on the microprocessor 2102, is very important.

The correlation between the sensed forehead temperature to an estimated body core temperature varies based on age, sex, and a febrile (pyretic) or hypothermic condition of the patient and intraday time of the reading. Accordingly, in some implementations, the multi-vital-sign capture system(s) 104 includes temperature estimation tables 2127 that are specific to the combinations and permutations of the various situations of the age, sex, and a febrile (pyretic) or hypothermic condition of the patient and the intraday time of the reading. For example, in one implementation, the multi-vital-sign capture system(s) 104 include a temperature estimation table 2127 for male humans of 3-10 years old, that are neither febrile nor hypothermic, for temperature readings taken between 10 am-2 pm. In another example, in another implementation, the multi-vital-sign capture system(s) 104 include a temperature estimation table 2127 for female humans of greater than 51 years of age, that are febrile and for temperature readings taken between 2 am-8 am.

Some implementations of the multi-vital-sign capture system 2100 include a solid-state image transducer 2128 that is operably coupled to the microprocessor 2102 and is configured to provide two or more images 2130 to a temporal-variation-amplifier 2132 and a biological vital sign generator 2134 in the microprocessor 2102 to estimate one or more biological vital signs 2136 that are displayed on the display device 2114.

The multi-vital-sign capture system 2100 includes any one of a pressure sensor 2138, a pressure cuff 2140, a micro dynamic light scattering (mDLS) sensor 2142 and/or a photoplethysmogram (PPG) sensor 2144 that provide signals to the biological vital sign generator 2134. The mDLS sensor uses a laser beam (singular wavelength) of light and a light detector on the opposite side of the finger to detect the extent of the laser beam that is scattered in the flesh of the finger, which indicates the amount of oxygen in blood in the fingertip. The PPG sensor uses projected light and a light detector on the opposite side of the finger to detect the extent of the laser beam that is absorbed in the flesh of the finger, which indicates the amount of oxygen in blood in the fingertip, which is also known as pulse oximetry. The pressure sensor 2138 is directly linked to the pressure cuff 2140. In some implementations, the multi-vital-sign capture system 2100 includes two mDLS sensors to ensure that at least one of the mDLS sensors provides a good quality signal. In some implementations, the biological vital sign generator 2134 generates blood pressure measurement (systolic and diastolic) from signals from the pressure sensor 2138, the finger pressure cuff 2140 and the mDLS sensor 2142. In some implementations, the biological vital sign generator 2134 generates SPO2 measurement and heart rate measurement from signals from the PPG sensor 2144. In some implementations, the biological vital sign generator 2134 generates respiration (breathing rate) measurement from signals from the mDLS sensor 2142. In some implementations, the biological vital sign generator 2134 generates blood flow measurement from signals from the mDLS sensor 2142. In some implementations, the biological vital sign generator 2134 generates heartrate variability from signals from the PPG sensor 2144. In some implementations, the body core temperature estimator 2118 is implemented in the biological vital sign generator 2134.

The multi-vital-sign capture system 2100 also includes a wireless communication subsystem 2146 or other external communication subsystem, such as an Ethernet port, that provides communication to the EMR data capture systems 100, 200 and 300 or other devices. In some implementations, the wireless communication subsystem 2146 is communication subsystem 2146 in FIG. 52. The wireless communication subsystem 2146 is operable to receive and transmit the estimated body core temperature 2120 and/or the biological vital sign(s) 2136.

In some implementations, the digital infrared sensor 2108 is a low noise amplifier, 17-bit ADC and powerful DSP unit through which high accuracy and resolution of the estimated body core temperature 2120 by the multi-vital-sign capture systems in FIG. 21-23, the apparatus that estimates a body core temperature in FIGS. 21-22 and 25, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000.

In some implementations, the digital infrared sensor 2108, 10-bit pulse width modulation (PWM) is configured to continuously transmit the measured temperature in range of −20 . . . 120° C., with an output resolution of 0.14° C. The factory default power on reset (POR) setting is SMBus. In some implementations, the digital infrared sensor 2108 is packaged in an industry standard TO-39 package.

In some implementations, the generated object and ambient temperatures are available in RAM of the digital infrared sensor 2108 with resolution of 0.01° C. The temperatures are accessible by 2 wire serial SMBus compatible protocol (0.02° C. resolution) or via 10-bit PWM (Pulse Width Modulated) output of the digital infrared sensor 2108.

In some implementations, the digital infrared sensor 2108 is factory calibrated in wide temperature ranges: −40 . . . 85° C. for the ambient temperature and −70 . . . 380° C. for the object temperature.

In some implementations of the digital infrared sensor 2108, the measured value is the average temperature of all objects in the Field Of View (FOV) of the sensor. In some implementations, the digital infrared sensor 2108 has a standard accuracy of ±0.5° C. around room temperatures, and in some implementations, the digital infrared sensor 2108 has an accuracy of ±0.2° C. in a limited temperature range around the human body core temperature.

These accuracies are only guaranteed and achievable when the sensor is in thermal equilibrium and under isothermal conditions (there are no temperature differences across the sensor package). The accuracy of the detector can be influenced by temperature differences in the package induced by causes like (among others): Hot electronics behind the sensor, heaters/coolers behind or beside the sensor or by a hot/cold object very close to the sensor that not only heats the sensing element in the detector but also the detector package. In some implementations of the digital infrared sensor 2108, the thermal gradients are measured internally and the measured temperature is compensated in consideration of the thermal gradients, but the effect is not totally eliminated. It is therefore important to avoid the causes of thermal gradients as much as possible or to shield the sensor from the thermal gradients.

In some implementations, the digital infrared sensor 2108 is configured for an object emissivity of 1, but in some implementations, the digital infrared sensor 2108 is configured for any emissivity in the range 0.1 . . . 1.0 without the need of recalibration with a black body.

In some implementations of the digital infrared sensor 2108, the PWM can be easily customized for virtually any range desired by the customer by changing the content of 2 EEPROM cells. Changing the content of 2 EEPROM cells has no effect on the factory calibration of the device. The PWM pin can also be configured to act as a thermal relay (input is To), thus allowing for an easy and cost effective implementation in thermostats or temperature (freezing/boiling) alert applications. The temperature threshold is programmable by the microprocessor 2102 of the multi-vital-sign capture system. In a multi-vital-sign capture system having a SMBus system the programming can act as a processor interrupt that can trigger reading all slaves on the bus and to determine the precise condition.

In some implementations, the digital infrared sensor 2108 has an optical filter (long-wave pass) that cuts off the visible and near infra-red radiant flux is integrated in the package to provide ambient and sunlight immunity. The wavelength pass band of the optical filter is from 5.5 to 14 μm.

In some implementations, the digital infrared sensor 2108 is controlled by an internal state machine, which controls the measurements and generations of the object and ambient temperatures and does the post-processing of the temperatures to output the body core temperatures through the PWM output or the SMBus compatible interface.

Some implementations of the multi-vital-sign capture system includes 2 IR sensors, the output of the IR sensors being amplified by a low noise low offset chopper amplifier with programmable gain, converted by a Sigma Delta modulator to a single bit stream and fed to a DSP for further processing. The signal is treated by programmable (by means of EEPROM contend) FIR and IIR low pass filters for further reduction of the bandwidth of the input signal to achieve the desired noise performance and refresh rate. The output of the IIR filter is the measurement result and is available in the internal RAM. 3 different cells are available: One for the on-board temperature sensor and 2 for the IR sensors. Based on results of the above measurements, the corresponding ambient temperature Ta and object temperatures To are generated. Both generated body core temperatures have a resolution of 0.01° C. The data for Ta and To is read in two ways: Reading RAM cells dedicated for this purpose via the 2-wire interface (0.02° C. resolution, fixed ranges), or through the PWM digital output (10 bit resolution, configurable range). In the last step of the measurement cycle, the measured Ta and To are rescaled to the desired output resolution of the PWM) and the regenerated data is loaded in the registers of the PWM state machine, which creates a constant frequency with a duty cycle representing the measured data.

In some implementations, the digital infrared sensor 2108 includes a SCL pin for Serial clock input for 2 wire communications protocol, which supports digital input only, used as the clock for SMBus compatible communication. The SCL pin has the auxiliary function for building an external voltage regulator. When the external voltage regulator is used, the 2-wire protocol for a power supply regulator is overdriven.

In some implementations, the digital infrared sensor 2108 includes a slave deviceA/PWM pin for Digital input/output. In normal mode the measured object temperature is accessed at this pin Pulse Width Modulated. In SMBus compatible mode the pin is automatically configured as open drain NMOS. Digital input/output, used for both the PWM output of the measured object temperature(s) or the digital input/output for the SMBus. In PWM mode the pin can be programmed in EEPROM to operate as Push/Pull or open drain NMOS (open drain NMOS is factory default). In SMBus mode slave deviceA is forced to open drain NMOS I/O, push-pull selection bit defines PWM/Thermal relay operation. The PWM/slave deviceA pin the digital infrared sensor 2108 operates as PWM output, depending on the EEPROM settings. When WPWM is enabled, after POR the PWM/slave deviceA pin is directly configured as PWM output. When the digital infrared sensor 2108 is in PWM mode, SMBus communication is restored by a special command. In some implementations, the digital infrared sensor 2108 is read via PWM or SMBus compatible interface. Selection of PWM output is done in EEPROM configuration (factory default is SMBus). PWM output has two programmable formats, single and dual data transmission, providing single wire reading of two temperatures (dual zone object or object and ambient). The PWM period is derived from the on-chip oscillator and is programmable.

In some implementations, the digital infrared sensor 2108 includes a VDD pin for External supply voltage and a VSS pin for ground.

The microprocessor 2102 has read access to the RAM and EEPROM and write access to 9 EEPROM cells (at addresses 0x00, 0x01, 0x02, 0x03, 0x04, 0x05*, 0x0E, 0x0F, 0x09). When the access to the digital infrared sensor 2108 is a read operation, the digital infrared sensor 2108 responds with 16 data bits and 8 bit PEC only if its own slave address, programmed in internal EEPROM, is equal to the SA, sent by the master. A slave feature allows connecting up to 127 devices (SA=0x00 . . . 0x07F) with only 2 wires. In order to provide access to any device or to assign an address to a slave device before slave device is connected to the bus system, the communication starts with zero slave address followed by low R/W bit. When the zero slave address followed by low R/W bit sent from the microprocessor 2102, the digital infrared sensor 2108 responds and ignores the internal chip code information.

In some implementations, two digital infrared sensors 2108 are not configured with the same slave address on the same bus.

In regards to bus protocol, after every received 8 bits, the slave device should issue ACK or NACK. When a microprocessor 2102 initiates communication, the microprocessor 2102 first sends the address of the slave and only the slave device which recognizes the address will ACK, the rest will remain silent. In case the slave device NACKs one of the bytes, the microprocessor 2102 stops the communication and repeat the message. A NACK could be received after the packet error code (PEC). A NACK after the PEC means that there is an error in the received message and the microprocessor 2102 attempts resending the message. PEC generation includes all bits except the START, REPEATED START, STOP, ACK, and NACK bits. The PEC is a CRC-8 with polynomial X8+X2+X1+1. The Most Significant Bit of every byte is transferred first.

In single PWM output mode the settings for PWM1 data only are used. The temperature reading can be generated from the signal timing as:

$T_{OUT} = {\left( {\frac{2t_{2}}{T} \times \left( {T_{O\;\_\;{MA}\; X} - T_{O\;\_\; M\;{IN}}} \right)} \right) + T_{O\;\_\; M\; I\; N}}$

where Tmin and Tmax are the corresponding rescale coefficients in EEPROM for the selected temperature output (Ta, object temperature range is valid for both Tobj1 and Tobj2 as specified in the previous table) and T is the PWM period. Tout is TO1, TO2 or Ta according to Config Register [5:4] settings.

The different time intervals t1 . . . t4 have following meaning:

t1: Start buffer. During t1 the signal is always high. t1=0.125 s×T (where T is the PWM period)

t2: Valid Data Output Band, 0 . . . ½T. PWM output data resolution is 10 bit.

t3: Error band—information for fatal error in EEPROM (double error detected, not correctable).

t3=0.25 s×T. Therefore a PWM pulse train with a duty cycle of 0.875 indicates a fatal error in EEPROM (for single PWM format). FE means Fatal Error.

In regards to a format for extended PWM, the temperature can be generated using the following equation:

$T_{{OUT}\; 1} = {\left( {\frac{4t_{2}}{T} \times \left( {T_{{MA}\; X\; 1} - T_{M\; I\; N\; 1}} \right)} \right) + T_{M\; I\; N\; 1}}$

-   -   For Data 2 field the equation is:

$T_{{OUT}\; 2} = {\left( {\frac{4t_{5}}{T} \times \left( {T_{M\;{AX}\; 2} - T_{M\; I\; N\; 2}} \right)} \right) + T_{M\; I\; N\; 2}}$

FIG. 22 is a block diagram of a multi-vital-sign capture system 2200 that includes a non-touch electromagnetic sensor with no temporal variation amplifier, according to an implementation. The multi-vital-sign capture system 2200 is one example of the multi-vital-sign capture system 104 and one example of the Multi-Parameter Sensor Box (MPSB) 502. The multi-vital-sign capture system 2200 includes a battery 2104, in some implementations a single button 2106, in some implementations a display device 2114, a non-touch electromagnetic sensor 2202 and an ambient air sensor 2122 that are operably coupled to the microprocessor 2102. The microprocessor 2102 is configured to receive a representation of an infrared signal 2116 of the forehead or other external source point from the non-touch electromagnetic sensor 2202. The microprocessor 2102 includes a body core temperature estimator 2118 that is configured to estimate the body core temperature 2212 of the subject from the representation of the electromagnetic energy of the external source point.

The multi-vital-sign capture system 2200 includes a pressure sensor 2138, a pressure cuff 2140, a mDLS sensor 2142 and a PPG sensor 2144 that provide signals to the biological vital sign generator 2134. The pressure sensor 2138 is directly linked to the pressure cuff 2140. In some implementations, the multi-vital-sign capture system 2200 includes two mDLS sensors to ensure that at least one of the mDLS sensors provides a good quality signal. In some implementations, the biological vital sign generator 2134 generates blood pressure measurement (systolic and diastolic) from signals from the pressure sensor 2138, the finger pressure cuff 2140 and the mDLS sensor 2142. In some implementations, the biological vital sign generator 2134 generates SPO2 measurement and heart rate measurement from signals from the PPG sensor 2144. In some implementations, the biological vital sign generator 2134 generates respiration (breathing rate) measurement from signals from the mDLS sensor 2142. In some implementations, the biological vital sign generator 2134 generates blood flow measurement from signals from the mDLS sensor 2142. In some implementations, the biological vital sign generator 2134 generates heartrate variability from signals from the PPG sensor 2144.

The body core temperature correlation table for all ranges of ambient temperatures provides best results because a linear or a quadratic relationship provide inaccurate estimates of body core temperature, yet a quartic relationship, a quintic relationship, sextic relationship, a septic relationship or an octic relationship provide estimates along a highly irregular curve that is far too wavy or twisting with relatively sharp deviations.

The non-touch electromagnetic sensor 2202 detects temperature in response to remote sensing of a surface a human or animal. In some implementations, the multi-vital-sign capture system having an infrared sensor is an infrared temperature sensor. All humans or animals radiate infrared energy. The intensity of this infrared energy depends on the temperature of the human or animal, thus the amount of infrared energy emitted by a human or animal can be interpreted as a proxy or indication of the body core temperature of the human or animal. The non-touch electromagnetic sensor 2202 measures the temperature of a human or animal based on the electromagnetic energy radiated by the human or animal. The measurement of electromagnetic energy is taken by the non-touch electromagnetic sensor 2202 which constantly analyzes and registers the ambient temperature. When the operator of apparatus in FIG. 22 holds the non-touch electromagnetic sensor 2202 about 5-8 cm (2-3 inches) from the forehead and activates the radiation sensor, the measurement is instantaneously measured. To measure a temperature using the non-touch electromagnetic sensor 2202, pushing the button 2106 causes a reading of temperature measurement from the non-touch electromagnetic sensor 2202 and in some implementations the measured body core temperature is thereafter displayed on the display device 2114. Various implementations of the non-touch electromagnetic sensor 2202 can be a digital infrared sensor, such as digital infrared sensor 2108 or an analog infrared sensor.

The body core temperature estimator 2118 correlates the temperatures sensed by the non-touch electromagnetic sensor 2202 to another temperature, such as a body core temperature of the subject, an axillary temperature of the subject, a rectal temperature of the subject and/or an oral temperature of the subject. The body core temperature estimator 2118 can be implemented as a component on a microprocessor, such as main processor 5002 in FIG. 50 or on a memory such as flash memory 5008 in FIG. 50.

The multi-vital-sign capture system 2200 also detects the body core temperature of a human or animal regardless of the room temperature because the measured temperature of the non-touch electromagnetic sensor 2202 is adjusted in reference to the ambient temperature in the air in the vicinity of the apparatus. The human or animal must not have undertaken vigorous physical activity prior to temperature measurement in order to avoid a misleading high temperature. Also, the room temperature should be moderate, 50° F. to 120° F.

The multi-vital-sign capture system 2200 provides a non-invasive and non-irritating means of measuring human or animal body core temperature to help ensure good health.

When evaluating results, the potential for daily variations in body core temperature can be considered. In children less than 6 months of age daily variation is small. In children 6 months to 4 years old the variation is about 1 degree. By age 6 variations gradually increase to 4 degrees per day. In adults there is less body core temperature variation.

The multi-vital-sign capture system 2200 also includes a wireless communication subsystem 2146 or other external communication subsystem, such as an Ethernet port, that provides communication to the EMR data capture systems 100, 200 and 300. In some implementations, the wireless communication subsystem 2146 is communication subsystem 2146 in FIG. 52.

FIG. 23 is a block diagram of a multi-vital-sign capture system 2300 that includes a non-touch electromagnetic sensor and that detects biological vital-signs from images captured by a solid-state image transducer, according to an implementation. The multi-vital-sign capture system 2300 is one example of the multi-vital-sign capture system 104 and one example of the Multi-Parameter Sensor Box (MPSB) 502 in FIG. 5. The multi-vital-sign capture system 2300 includes a battery 2104, in some implementations a single button 2106, in some implementations a display device 2114, a non-touch electromagnetic sensor 2202 and an ambient air sensor 2122 that are operably coupled to the microprocessor 2102. The microprocessor 2102 is configured to receive a representation of an infrared signal 2116 of the forehead or other external source point from the non-touch electromagnetic sensor 2202. The microprocessor 2102 includes a body core temperature estimator 2118 that is configured to estimate the body core temperature 2212 of the subject from the representation of the electromagnetic energy of the external source point. The multi-vital-sign capture system 2300 includes a solid-state image transducer 2128 that is operably coupled to the microprocessor 2102 and is configured to provide two or more images 2130 to the microprocessor 2102.

The multi-vital-sign capture system 2300 include a pressure sensor 2138, a pressure cuff 2140, a mDLS sensor 2142 and a PPG sensor 2144 that provide signals to the biological vital sign generator 2134. The pressure sensor 2138 is directly linked to the pressure cuff 2140. In some implementations, the multi-vital-sign capture system 2300 includes two mDLS sensors to ensure that at least one of the mDLS sensors provides a good quality signal. In some implementations, the biological vital sign generator 2134 generates blood pressure measurement (systolic and diastolic) from signals from the pressure sensor 2138, the finger pressure cuff 2140 and the mDLS sensor 2142. In some implementations, the biological vital sign generator 2134 generates SPO2 measurement and heart rate measurement from signals from the PPG sensor 2144. In some implementations, the biological vital sign generator 2134 generates respiration (breathing rate) measurement from signals from the mDLS sensor 2142. In some implementations, the biological vital sign generator 2134 generates blood flow measurement from signals from the mDLS sensor 2142. In some implementations, the biological vital sign generator 2134 generates heartrate variability from signals from the PPG sensor 2144.

FIG. 24 is a block diagram of an apparatus 2400 to generate a predictive analysis of vital signs, according to an implementation. The apparatus 2400 can be implemented on the Multi-Parameter Sensor box (MPSB) 402 in FIG. 4, the Non-Contact Human Multi-Vital Sign (NCPMVS) device 404 in FIG. 4, the Multi-Parameter Sensor box (MPSB) 502 in FIG. 5 or the Non-Contact Human Multi-Vital Sign (NCPMVS) device 503 in FIG. 5, the sensor management component 602 in FIG. 6, the microprocessor 620 in FIG. 6, the multi-vital-sign finger cuff 506 in FIG. 5 and FIG. 7, the microprocessor 702 in FIG. 7, controller 820 in FIG. 8, the microprocessor 2102 in FIGS. 21-23 and 25 and/or main processor 5002 in FIG. 50. In apparatus 2400, heartrate data 2402 (such as heartrate 3910 in FIG. 39), respiratory rate data 2404 (such as respiratory rate 3916 in FIG. 39), estimated body core temperature data 2406 (such as estimated body core temperature 2120 in FIG. 21 or estimated body core temperature 2212 in FIG. 22-24), blood pressure data 2408 (such as blood pressure 3922 in FIG. 39), EKG data 2410 (such as EKG 3928 in FIG. 39) and/or SPO2 data 2412 is received by a predictive analysis component 2414 that evaluates the data 2402, 2404, 2406, 2408, 2410 and/or 2412 in terms of percentage of change over time. More specifically, the relative change and the rate of change or change in comparison to an established pattern that is described in terms of frequency and amplitude. When the percentage change over time exceeds a predetermined threshold, a flag 2416 is set to indicate an anomaly. The flag 2416 can be transmitted to the EMR/clinical data repository 144, as shown in FIG. 1-3.

4. Non-Touch Table-Based Temperature Correlation Thermometers

FIG. 25 is a block diagram of an apparatus 2500 that includes a digital infrared sensor with no other vital sign detection components, according to an implementation. The apparatus 2500 is one example of the Non-Contact Human Multi-Vital Sign (NCPMVS) device 503. The apparatus 2500 includes a battery 2104, in some implementations a single button 2106, in some implementations a display device 2114, a digital infrared sensor 2108 and an ambient air sensor 2122 that are operably coupled to the microprocessor 2102. The microprocessor 2102 is configured to receive a representation of an infrared signal 2116 of the forehead or other external source point from the digital infrared sensor 2108. The microprocessor 2102 includes a body core temperature estimator 2118 that is configured to estimate the body core temperature 2120 of the subject from the representation of the electromagnetic energy of the external source point.

The apparatus 2500 does not include a pressure sensor 2138, a pressure cuff 2140, a mDLS sensor 2142 and a PPG sensor 2144 that provide signals to a biological vital sign generator 2134.

In some implementations, the apparatus 2500 also includes a wireless communication subsystem 2146 or other external communication subsystem, such as an Ethernet port, that provides communication to the EMR data capture systems 100, 200 and 300 or other devices. In some implementations, the wireless communication subsystem 2146 is communication subsystem 2146 in FIG. 52. The wireless communication subsystem 2146 is operable to receive and transmit the estimated body core temperature 2120 and/or the biological vital sign(s).

The apparatus 2500 also includes a wireless communication subsystem 2146 or other external communication subsystem, such as an Ethernet port, that provides communication to the EMR data capture apparatus 1800 or other devices. In some implementations, the wireless communication subsystem 2146 is communication subsystem 2146 in FIG. 52. The wireless communication subsystem 2146 is operable to receive and transmit the estimated body core temperature 2120 and/or the biological vital sign(s).

In regards to the structural relationship of the digital infrared sensor 2108 and the microprocessor 2102 in FIGS. 21-23 and 25, heat radiation on the digital infrared sensor 2108 from any source such as the microprocessor 2102 or heat sink, will distort detection of infrared energy by the digital infrared sensor 2108. In order to prevent or at least reduce heat transfer between the digital infrared sensor 2108 and the microprocessor 2102, the apparatus in FIGS. 21-23 and 25 are low-powered devices and thus low heat-generating devices that are also powered by a battery 2104; and that are only used for approximately a 5 second period of time for each measurement (1 second to acquire the temperature samples and generate the body core temperature result, and 4 seconds to display that result to the operator) so there is little heat generated by the apparatus in FIGS. 21-23 and 25 in active use.

The internal layout of the apparatus in FIGS. 21-23 and 25 minimizes as practically as possible the digital infrared sensor as far away in distance from all other components such the microprocessor (620, 702 and 2102) or controller 820 within the practical limitations of the industrial design of the apparatus in FIGS. 21-23 and 25.

More specifically, to prevent or at least reduce heat transfer between the digital infrared sensor 2108 and the microprocessor (620, 702 and 2102) or controller 820 in some implementations the digital infrared sensor 2108 is isolated on a separate PCB from the PCB that has the microprocessor 620, 702 and 2102) or controller 820, and the two PCBs are connected by only a connector that has 4 pins. The minimal connection of the single connector having 4 pins reduces heat transfer from the microprocessor (620, 702 and 2102) or controller 820 to the digital infrared sensor 2108 through the electrical connector and through transfer that would occur through the PCB material if the digital infrared sensor 2108 and the microprocessor 2102 were mounted on the same PCB.

In some implementations, the apparatus in FIGS. 21-22 and 25 includes only one printed circuit board, in which case the printed circuit board includes the microprocessor 2102 and the digital infrared sensor 2108 or the non-touch electromagnetic sensor 2202 are mounted on the singular printed circuit board. In some implementations, the apparatus in FIGS. 21-22 and 25 includes two printed circuit boards, such as a first printed circuit board and a second printed circuit board in which the microprocessor 2102 is on the first printed circuit board and the digital infrared sensor 2108 or non-touch electromagnetic sensor 2202 are on the second printed circuit board. In some implementations, the apparatus in FIGS. 21-22 and 25 includes only one display device 2114, in which case the display device 2114 includes not more than one display device 2114. In some implementations, the display device 2114 is a liquid-crystal diode (LCD) display device. In some implementations, the display device 2114 is a light-emitting diode (LED) display device. In some implementations, the apparatus in FIGS. 21-23 and 25 includes only one battery 2104.

FIG. 26 is a block diagram of a digital infrared sensor 2600, according to an implementation. The digital infrared sensor 2600 contains a single thermopile sensor 2602 that senses only infrared electromagnetic energy 2604. The digital infrared sensor 2600 contains a CPU control block 2606 and an ambient temperature sensor 2608, such as a thermocouple. The single thermopile sensor 2602, the ambient temperature sensor 2608 and the CPU control block 2606 are on separate silicon substrates 2610, 2612 and 2614 respectively. The CPU control block 2606 digitizes the output of the single thermopile sensor 2602 and the ambient temperature sensor 2608.

The digital infrared sensor 2600 has a Faraday cage 2616 surrounding the single thermopile sensor 2602, the CPU control block 2606 and the ambient temperature sensor 2608 to prevent electromagnetic (EMF) interference in the single thermopile sensor 2602, the CPU control block 2606 and the ambient temperature sensor 2608 that shields the components in the Faraday cage 2616 from outside electromagnetic interference, which improves the accuracy and the repeatability of a device that estimates body core temperature from the ambient and object temperature generated by the digital infrared sensor 2600. The digital IR sensor 2600 also requires less calibration in the field after manufacturing, and possibly no calibration in the field after manufacturing because in the digital infrared sensor 2600, the single thermopile sensor 2602, the CPU control block 2606 and the ambient temperature sensor 2608 are in close proximity to each other, which lowers temperature differences between the single thermopile sensor 2602, the CPU control block 2606 and the ambient temperature sensor 2608, which minimizes or eliminates calibration drift over time because they are based on the same substrate material and exposed to the same temperature and voltage variations. In comparison, conventional infrared temperature sensors do not include a Faraday cage 2616 that surrounds the single thermopile sensor 2602, the CPU control block 2606 and the ambient temperature sensor 2608. The Faraday cage 2616 can be a metal box or a metal mesh box. In the implementation where the Faraday cage 2616 is a metal box, the metal box has an aperture where the single thermopile sensor 2602 is located so that the field of view of the infrared electromagnetic energy 2604 is not affected by the Faraday cage 2616 so that the infrared electromagnetic energy 2604 can pass through the Faraday cage 2616 to the single thermopile sensor 2602. In the implementation where the Faraday cage 2616 is a metal box, the metal box has an aperture where the ambient temperature sensor 2608 is located so that the atmosphere can pass through the Faraday cage 2616 to the ambient temperature sensor 2608. In other implementations the ambient air temperature sensor 2608 does not sense the temperature of the atmosphere, but instead senses the temperature of the sensor substrate (silicon) material and surrounding materials because the ambient temperature sensor 2608 and the target operating environment temperature are required to be as close as possible in order to reduce measurement error, i.e. the ambient temperature sensor 2608 is to be in thermal equilibrium with the target operating environment.

In some further implementations, the Faraday cage 2616 of the digital infrared sensor 2600 also includes an multichannel analogue-to-digital converter (ADC) 2618 that digitizes an analogue signal from the single thermopile sensor 2602. The ADC 2618 also digitizes an analogue signal from the ambient temperature sensor 2608. In another implementation where the ADC is not a multichannel ADC, separate ADCs are used to digitize the analogue signal from the single thermopile sensor 2602 and the analogue signal from the ambient temperature sensor 2608. There is no ADC between the digital infrared sensor 2600 and microprocessor(s), main processor(s) and controller(s) that are outside the digital IR sensor 2600, such as the microprocessor 2102 in FIG. 21.

The single thermopile sensor 2602 of the digital infrared sensor 2600 is tuned to be most sensitive and accurate to the human body core temperature range, such as forehead surface temperature range of 25° C. to 39° C. The benefits of the digital IR sensor 2600 in comparison to conventional analogue infrared temperature sensors include minimization of the temperature difference between the analogue and digital components effects on calibration parameters (when the temperature differences are close there is a smaller ΔT which mimics the calibration environment) and reduction of EMC interference in the datalines. The digital infrared sensor 2600 outputs a digital representation of the surface temperature in absolute Kelvin degrees (° K) that is presented at a digital readout port of the digital infrared sensor 2600. The digital representation of the surface temperature is also known as the body surface temperature in FIG. 5-8, digital readout signal 2111 in FIGS. 21-23 and 25, digital signal that is representative of an infrared signal of a forehead temperature that is detected by the digital infrared sensor in FIG. 29, the body core temperature in FIG. 30, the temperature measurement in FIG. 31, the sensed forehead temperature in FIGS. 19, 21-22 and 25, 29 and 32 and the numerical representation of the electromagnetic energy of the external source point in FIG. 49.

The digital infrared sensor 2600 is not an analog device or component, such as a thermistor or a resistance temperature detector (RTD). Because the digital infrared sensor 2600 is not a thermistor, there is no need or usefulness in receiving a reference signal of a resister and then determining a relationship between the reference signal and a temperature signal to compute the surface temperature. Furthermore, the digital infrared sensor 2600 is not an array of multiple transistors as in complementary metal oxide (CMOS) devices or charged coupled (CCD) devices. None of the subcomponents in the digital infrared sensor 2600 detect electromagnetic energy in wavelengths of the human visible spectrum (380 nm-750 nm). Neither does the digital infrared sensor 2600 include an infrared lens.

5. Interoperability Device Manager Component of an EMR System

FIG. 27 is a block diagram of a system of interoperability device manager component 126, according to an implementation. The interoperability device manager component 126 includes a device manager 2702 that connects one or more multi-vital-sign capture system(s) 104 and middleware 2706. The multi-vital-sign capture system(s) 104 are connected to the device manager 2702 through via a plurality of services, such as a chart service 2708, an observation service 2710, a patient service 2712, a user service and/or an authentication service 2716 to a bridge 2718 in the interoperability device manager 2702. The multi-vital-sign capture system(s) 104 are connected to the device manager 2702 to a plurality of maintenance function components 2720, such as push firmware 2722, a push configuration component 2724 and/or a keepalive signal component 2726. The keepalive signal component 2726 is coupled to the middleware 2706. In some implementations, the APIs 2730, 2732, 2734 and 2736 are health date APIs, observation APIs, electronic health record (EHR) or electronic medical record (EMR) APIs.

The bridge 2718 is operably coupled to a greeter component 2728. The greeter component 2728 synchronizes date/time of the interoperability device manager 2702, checks device log, checks device firmware, checks device configuration and performs additional security. The greeter component 2728 is coupled to the keepalive signal component 2726 through a chart application program interface component 2730, a patient application program interface component 2732, a personnel application program interface component 2734 and/or and authentication application program interface component 2736. All charted observations from the chart application program interface component 2730 are stored in a diagnostics log 2738 of a datastore 2740. The datastore 2740 also includes interoperability device manager settings 2742 for the application program interface components 2730, 2732, 2734 and/or 2736, current device configuration settings 2744, current device firmware 2746 and a device log 2748.

The interoperability device manager 2702 also includes a provision device component 2750 that provides network/WiFi® Access, date/time stamps, encryption keys—once for each of the multi-vital-sign capture system(s) 104 for which each multi-vital-sign capture system(s) 104 is registered and marked as ‘active’ in the device log 2748. The provision device component 2750 activates each new multi-vital-sign capture system(s) 104 on the interoperability device manager component 126 through a device activator 2752.

6. Methods of Multi-Vital-Sign Capture Systems Having an Infrared Sensor

In this section, the particular methods performed by FIGS. 21-23 and 25 are described by reference to a series of flowcharts.

FIG. 28 is a flowchart of a method 2800 to perform real time quality check on finger cuff data, according to an implementation. The method 2800 uses signals from PPG and mDLS sensors to perform quality check. The method 2800 can be performed by the Multi-Parameter Sensor box (MPSB) 402 in FIG. 4, the MPSB 502 in FIG. 5, the sensor management component 602 in FIG. 6, the microprocessor 620 in FIG. 6, the multi-vital-sign finger cuff 506 in FIG. 5 and FIG. 7, the microprocessor 702 in FIG. 7, controller 820 in FIG. 8, the microprocessor 2102 in FIGS. 21-23 and 25 and/or main processor 5002 in FIG. 50.

In method 2800, raw data 2802 is received from a PPG sensor, such as PPG sensor in the multi-vital-sign finger cuff 506 in FIG. 5-7, 842 in FIG. 8 and/or 2144 in FIG. 21-23, raw data 2804 is received from two mDLS sensors, such as mDLS sensor in the multi-vital-sign finger cuff 506 in FIG. 5-7, 844 in FIG. 8, and/or 2142 in FIG. 21-23, raw data 2806 is received from pressure cuff, such as multi-vital-sign finger cuff 406 in FIG. 4, pneumatic engine 507 in FIG. 5-7, cuff 850 in FIG. 8, the pressure sensor 908 in FIG. 9, and/or the pressure sensor 2138 in FIG. 21-23, raw data 2824 is received from an accelerometer and raw data 2832 is received from a three-axis gyroscope. The raw data 2806 received from the pressure cuff can be received from the pneumatic pressure sensor 908 in FIG. 9.

The raw data 2802 that is received from the PPG sensor is analyzed in PPG signal processing 2808, the raw data 2804 that is received from the mDLS sensors is analyzed in mDLS signal processing 2810, the raw data 2806 that is received from the pressure cuff is analyzed in cuff pressure processing 2812, the raw data 2824 that is received from the accelerometer is analyzed in accelerometer processing 2826 and the raw data 2832 that is received from the three axis gyroscope is analyzed in gyroscope processing 2834. If the analysis in the PPG signal processing 2808 and the mDLS signal processing 2810 indicates a poor signal-to-noise ratio 2814 in the raw data 2802 that is received from the PPG sensor or the raw data 2804 that is received from the mDLS sensors, the measurement is ended 2815. If the analysis in the PPG signal processing 2808 and the mDLS signal processing 2810 indicates a good signal-to-noise ratio 2814 in both the raw data 2802 that is received from the PPG sensor and the raw data 2804 that is received from the mDLS sensors, then a waveform analysis 2818 is performed on both the raw data 2802 that is received from the PPG sensor and the raw data 2804 that is received from the mDLS sensors. If the analysis in the cuff pressure processing 2812 indicates the bladder of the finger occlusion cuff can not be inflated to a required pressure or that the required amount of pressure can not be maintained in the bladder of the multi-vital-sign finger cuff 2816 then the measurement is ended 2815. If the analysis in the accelerometer processing 2826 indicates unreliable data from the accelerometer, then the measurement is ended 2815. If the analysis in the three axis gyroscope processing 2834 indicates unreliable data from the three axis gyroscope, then the measurement is ended 2815.

From the waveform analysis 2818 that is performed on both the raw data 2802 that is received from the PPG sensor and the raw data 2804 that is received from the mDLS sensors, flags indicating that status of heartrate, respiratory rate and/or are generated 2820. From the cuff pressure processing 2812, flags indicating the blood pressure (diastolic and systolic) are generated 2822. From the accelerometer processing 2826, flags indicating the quality of the accelerometer data 2824 are generated 2830. From the three axis gyroscope processing 2834, flags indicating the quality of the three axis gyroscope data 2832 are generated 2838.

FIG. 29 is a flowchart of a method 2900 to estimate a body core temperature from a digital infrared sensor, according to an implementation. Method 2900 includes receiving from the digital readout ports of a digital infrared sensor a digital signal that is representative of an infrared signal of a forehead temperature that is detected by the digital infrared sensor, at block 2902. No signal that is representative of the infrared signal is received from an analog infrared sensor.

Method 2900 also includes estimating a body core temperature from the digital signal that is representative of the infrared signal, at block 2904.

FIG. 30 is a flowchart of a method 3000 to display body core temperature color indicators, according to an implementation of three colors. Method 3000 provides color rendering to indicate a general range of a body core temperature.

Method 3000 includes receiving the body core temperature (such as digital readout signal 2111 that is representative of the infrared signal 2116 of the forehead in FIG. 21), at block 3001.

Method 3000 also includes determining whether or not the body core temperature is in a first range, such as a range of 32.0° C. and 37.3° C., at block 3002. If the body core temperature is in the first range, then the color is set to ‘amber’ to indicate a body core temperature that is low, at block 3004 and a lighting emitting diode (LED) or the background of the display is activated in accordance with the color, at block 3006.

If the body core temperature is not the first range, then method 3000 also includes determining whether or not the body core temperature is in a second range that is immediately adjacent and higher than the first range, such as a range of 37.4° C. and 38.0° C., at block 3008. If the body core temperature is in the second range, then the color is set to green to indicate no medical concern, at block 3010 and the LED or the background of the display is activated in accordance with the color, at block 3006.

If the body core temperature is not the second range, then method 3000 also includes determining whether or not the body core temperature is over the second range, at block 3012. If the body core temperature is over the second range, then the color is set to ‘red’ to indicate alert, at block 3012 and the LED or the background is activated in accordance with the color, at block 3006.

Method 3000 assumes that body core temperature is in gradients of 10ths of a degree. Other body core temperature range boundaries are used in accordance with other gradients of body core temperature sensing.

In some implementations, some pixels in the LED or the display are activated as an amber color when the body core temperature is between a first range of 36.3° C. and 37.3° C. (97.3° F. to 99.1° F.), some pixels in the display are activated as a green when the body core temperature is between a second range of 37.4° C. and 37.9° C. (99.3° F. to 100.2° F.), the LED or some pixels in the display are activated as a red color when the body core temperature is greater than the second range (a least 38° C. (100.4° F.)).

FIG. 31 is a flowchart of a method 3100 to manage power in a non-touch device having a digital infrared sensor, according to an implementation. The method 3100 manages power in the device, such as multi-vital-sign capture systems and multi-vital-sign capture systems in FIGS. 4-8 and 21-23 and FIG. 50, in order to reduce heat pollution in the digital infrared sensor.

To prevent or at least reduce heat transfer between the digital infrared sensor 2108 and the microprocessor 2102, main processor 5002 in FIG. 50, the components of the multi-vital-sign capture systems in FIG. 21-23, the apparatus that estimates a body core temperature in FIGS. 21-22 and 25, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000 are power controlled, i.e. sub-systems are turned on and off, and the sub-systems are only activated when needed in the measurement and display process, which reduces power consumption and thus heat generation by the microprocessor 2102, or main processor 5002 in FIG. 50, of the multi-vital-sign capture systems in FIG. 21-23, the apparatus that estimates a body core temperature in FIG. 22-24, the apparatus of variation amplification in FIG. 34-42, the multi-vital-sign capture system 5000, respectively. When not in use, at block 3102, the multi-vital-sign capture systems in FIG. 21-23, the apparatus that estimates a body core temperature in FIGS. 21-22 and 25, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000 are completely powered-off, at block 3104 (including the main PCB having the microprocessor 2102, main processor 5002 in FIG. 50 and the sensor PCB having the digital infrared sensor 2108) and not drawing any power, other than a power supply, i.e. a boost regulator, which has the effect that the multi-vital-sign capture systems in FIG. 3-21, the apparatus that estimates a body core temperature in FIG. 22-24, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000 draw only micro-amps from the battery 2104 while in the off state, which is required for the life time requirement of 3 years of operation, but which also means that in the non-use state there is very little powered circuitry in the multi-vital-sign capture systems in FIG. 21-23, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000 and therefore very little heat generated in the multi-vital-sign capture systems in FIG. 21-23, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000.

When the multi-vital-sign capture systems in FIGS. 21-22 and 24, the apparatus that estimates a body core temperature in FIGS. 22-23 and 24, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000 are started by the operator, at block 3106, only the microprocessor 2102, microprocessor 2102, microprocessor 5002. In FIG. 50, main processor 5002 in FIG. 50, digital infrared sensor 2108, and in some implementations low power LCD (e.g. display device 2114) are turned on for the first 1 second, at block 3108, to take the temperature measurement via the digital infrared sensor 2108 and generate the body core temperature result via the microprocessor 2102 in FIGS. 21-22 and 25, main processor 5002 in FIG. 50, at block 3110. In this way, the main heat generating components (the display device 2114, the main PCB having the microprocessor 2102 and the sensor PCB having the digital infrared sensor 2108), the display back-light and the body core temperature traffic light) are not on and therefore not generating heat during the critical start-up and measurement process, no more than 1 second. After the measurement process of block 3110 has been completed, the digital infrared sensor 2108 is turned off, at block 3112, to reduce current usage from the batteries and heat generation, and also the display back-light and temperature range indicators are turned on, at block 3114.

The measurement result is displayed for 4 seconds, at block 3116, and then the multi-vital-sign capture systems in FIG. 21-23, the apparatus that estimates a body core temperature in FIG. 22-24, the apparatus of variation amplification in FIG. 34-42 and the multi-vital-sign capture system 5000 are put in low power-off state, at block 3118.

In some implementations of methods and apparatus of FIG. 21-50 an operator can take the temperature of a subject and from the temperatures to estimate the temperature at a number of other locations of the subject.

The correlation of action can include a calculation based on Formula 1: T _(body) =|f _(stb)(T _(surface temp) +f _(ntc)(T _(ntc)))+F4_(body)|   Formula 1

where T_(body) is the temperature of a body or subject

where f_(stb) is a mathematical formula of a surface of a body

where f_(ntc) is mathematical formula for ambient temperature reading

where T_(surface temp) is a surface temperature estimated from the sensing.

where T_(ntc) is an ambient air temperature reading

where F4_(body) is a calibration difference in axillary mode, which is stored or set in a memory of the apparatus either during manufacturing or in the field. The apparatus also sets, stores and retrieves F4_(oral), F4_(core), and F4_(rectal) in the memory.

f_(ntc)(T_(ntc)) is a bias in consideration of the temperature sensing mode. For example f_(axillary)(T_(axillary))=0.2° C., f_(oral)(T_(oral))=0.4° C., f_(rectal)(T_(rectal))=0.5° C. and f_(core)(T_(core))=0.3° C.

7. Biological Vital Sign Motion Amplification Detectors

Apparatus in FIG. 34-42 use spatial and temporal signal processing to generate a biological vital sign from a series of digital images.

FIG. 34 is a block diagram of an apparatus 3400 of variation amplification, according to an implementation. Apparatus 3400 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate biological vital signs.

In some implementations, apparatus 3400 includes a forehead skin-pixel-identification module 3402 that identifies pixel-values that are representative of the skin in two or more images 3404. The pixel-values are the values of the pixels in the images 3404. In some implementations the images 3404 are frames of a video. The forehead skin-pixel-identification module 3402 performs block 4302 in FIG. 43. Some implementations of the forehead skin-pixel-identification module 3402 perform an automatic seed point based clustering process on the two or more images 3404. In some implementations, apparatus 3400 includes a frequency filter 3406 that receives the output of the forehead skin-pixel-identification module 3402 and applies a frequency filter to the output of the forehead skin-pixel-identification module 3402. The frequency filter 3406 performs block 4304 in FIG. 43 to process the images 3404 in the frequency domain. In implementations where the apparatus in FIG. 34-42 or the methods in FIG. 43-47 are implemented on multi-vital-sign capture systems and multi-vital-sign capture systems having an infrared sensor in FIG. 21-22, the images 3404 in FIG. 34-42 are the images 2130 in FIG. 21-23. In some implementations the apparatus in FIG. 34-40 or the methods in FIG. 43-47 are implemented on the multi-vital-sign capture system 5000 in FIG. 50.

In some implementations, apparatus 3400 includes a regional facial clusterial module 3408 that includes a spatial clusterer that is applied to the output of the frequency filter 3406. The regional facial clusterial module 3408 performs block 4306 in FIG. 43. In some implementations the regional facial clusterial module 3408 includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's apparatus or seed point based clustering.

In some implementations, apparatus 3400 includes a frequency-filter 3410 that applies a frequency filter to the output of the regional facial clusterial module 3408. The frequency-filter 3410 performs block 4308 in FIG. 43. In some implementations, the frequency-filter 3410 is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter. Some implementations of frequency-filter 3410 includes de-noising (e.g. smoothing of the data with a Gaussian filter). The forehead skin-pixel-identification module 3402, the frequency filter 3406, the regional facial clusterial module 3408 and the frequency-filter 3410 amplify temporal variations (as a temporal-variation-amplifier) in the two or more images 3404.

In some implementations, apparatus 3400 includes a temporal-variation identifier 3412 that identifies temporal variation of the output of the frequency-filter 3410. Thus, the temporal variation represents temporal variation of the images 3404. The temporal-variation identifier 3412 performs block 4310 in FIG. 43.

In some implementations, apparatus 3400 includes a biological vital-sign generator 3414 that generates one or more biological vital sign(s) 3416 from the temporal variation. The biological vital sign(s) 3416 are displayed for review by a healthcare worker or stored in a volatile or nonvolatile memory for later analysis, or transmitted to other devices for analysis.

Fuzzy clustering is a class of processes for cluster analysis in which the allocation of data points to clusters is not “hard” (all-or-nothing) but “fuzzy” in the same sense as fuzzy logic. Fuzzy logic being a form of many-valued logic which with reasoning that is approximate rather than fixed and exact. In fuzzy clustering, every point has a degree of belonging to clusters, as in fuzzy logic, rather than belonging completely to just one cluster. This, points on the edge of a cluster, may be in the cluster to a lesser degree than points in the center of cluster. Any point x has a set of coefficients giving the degree of being in the kth cluster w_(k)(x). With fuzzy c-means, the centroid of a cluster is the mean of all points, weighted by a degree of belonging of each point to the cluster:

$c_{k} = {\frac{\sum_{x}{{w_{k}(x)}^{m}x}}{\sum_{x}{w_{k}(x)}^{m}}.}$

The degree of belonging, w_(k)(x), is related inversely to the distance from x to the cluster center as calculated on the previous pass. The degree of belonging, w_(k)(x) also depends on a parameter m that controls how much weight is given to the closest center.

k-means clustering is a process of vector quantization, originally from signal processing, that is popular for cluster analysis in data mining, k-means clustering partitions n observations into k clusters in which each observation belongs to the cluster with the nearest mean, serving as a prototype of the cluster. This results in a partitioning of the data space into Voronoi cells. A Voronoi Cell being a region within a Voronoi Diagram that is a set of points which is specified beforehand. A Voronoi Diagram is a technique of dividing space into a number of regions, k-means clustering uses cluster centers to model the data and tends to find clusters of comparable spatial extent, like K-means clustering, but each data point has a fuzzy degree of belonging to each separate cluster.

An expectation-maximization process is an iterative process for finding maximum likelihood or maximum a posteriori (MAP) estimates of parameters in statistical models, where the model depends on unobserved latent variables. The expectation-maximization iteration alternates between performing an expectation step, which creates a function for the expectation of the log-likelihood evaluated using the current estimate for the parameters, and a maximization step, which computes parameters maximizing the expected log-likelihood found on the expectation step. These parameter-estimates are then used to determine the distribution of the latent variables in the next expectation step.

The expectation maximization process seeks to find the maximization likelihood expectation of the marginal likelihood by iteratively applying the following two steps:

1. Expectation step (E step): Calculate the expected value of the log likelihood function, with respect to the conditional distribution of Z given X under the current estimate of the parameters θ^((t)): Q(θ|θ^((t)))=E _(Z|X,θ) _((t)) [log L(θ;X,Z)]

2. Maximization step (M step): Find the parameter that maximizes this quantity:

$\theta^{({t + 1})} = {\underset{\theta}{argmax}{Q\left( \theta \middle| \theta^{(t)} \right)}}$

Note that in typical models to which expectation maximization is applied:

1. The observed data points X may be discrete (taking values in a finite or countably infinite set) or continuous (taking values in an uncountably infinite set). There may in fact be a vector of observations associated with each data point.

2. The missing values (aka latent variables) Z are discrete, drawn from a fixed number of values, and there is one latent variable per observed data point.

3. The parameters are continuous, and are of two kinds: Parameters that are associated with all data points, and parameters associated with a particular value of a latent variable (i.e. associated with all data points whose corresponding latent variable has a particular value).

The Fourier Transform is an important image processing tool which is used to decompose an image into its sine and cosine components. The output of the transformation represents the image in the Fourier or frequency domain, while the input image is the spatial domain equivalent. In the Fourier domain image, each point represents a particular frequency contained in the spatial domain image.

The Discrete Fourier Transform is the sampled Fourier Transform and therefore does not contain all frequencies forming an image, but only a set of samples which is large enough to fully describe the spatial domain image. The number of frequencies corresponds to the number of pixels in the spatial domain image, i.e. the image in the spatial and Fourier domains are of the same size.

For a square image of size N×N, the two-dimensional DFT is given by:

${F\left( {k,l} \right)} = {\sum\limits_{i = 0}^{N - 1}{\sum\limits_{j = 0}^{N - 1}{{f\left( {i,j} \right)}e^{{- \iota}\; 2{\pi{({\frac{ki}{N} + \frac{lj}{N}})}}}}}}$

where f(a,b) is the image in the spatial domain and the exponential term is the basis function corresponding to each point F(k,l) in the Fourier space. The equation can be interpreted as: the value of each point F(k,l) is obtained by multiplying the spatial image with the corresponding base function and summing the result.

The basis functions are sine and cosine waves with increasing frequencies, i.e. F(0,0) represents the DC-component of the image which corresponds to the average brightness and F(N−1,N−1) represents the highest frequency.

A high-pass filter (HPF) is an electronic filter that passes high-frequency signals but attenuates (reduces the amplitude of) signals with frequencies lower than the cutoff frequency. The actual amount of attenuation for each frequency varies from filter to filter. A high-pass filter is usually modeled as a linear time-invariant system. A high-pass filter can also be used in conjunction with a low-pass filter to make a bandpass filter. The simple first-order electronic high-pass filter is implemented by placing an input voltage across the series combination of a capacitor and a resistor and using the voltage across the resistor as an output. The product of the resistance and capacitance (R×C) is the time constant (z); the product is inversely proportional to the cutoff frequency f_(c), that is:

$f_{c} = {\frac{1}{2\pi\;\tau} = \frac{1}{2\pi\;{RC}}}$

where f_(c) is in hertz, τ is in seconds, R is in ohms, and C is in farads.

A low-pass filter is a filter that passes low-frequency signals and attenuates (reduces the amplitude of) signals with frequencies higher than the cutoff frequency. The actual amount of attenuation for each frequency varies depending on specific filter design. Low-pass filters are also known as high-cut filter, or treble cut filter in audio applications. A low-pass filter is the opposite of a high-pass filter. Low-pass filters provide a smoother form of a signal, removing the short-term fluctuations, and leaving the longer-term trend. One simple low-pass filter circuit consists of a resistor in series with a load, and a capacitor in parallel with the load. The capacitor exhibits reactance, and blocks low-frequency signals, forcing the low-frequency signals through the load instead. At higher frequencies the reactance drops, and the capacitor effectively functions as a short circuit. The combination of resistance and capacitance gives the time constant of the filter. The break frequency, also called the turnover frequency or cutoff frequency (in hertz), is determined by the time constant.

A band-pass filter is a device that passes frequencies within a certain range and attenuates frequencies outside that range. These filters can also be created by combining a low-pass filter with a high-pass filter. Bandpass is an adjective that describes a type of filter or filtering process; bandpass is distinguished from passband, which refers to the actual portion of affected spectrum. Hence, a dual bandpass filter has two passbands. A bandpass signal is a signal containing a band of frequencies not adjacent to zero frequency, such as a signal that comes out of a bandpass filter.

FIG. 35 is a block diagram of an apparatus 3500 of variation amplification, according to an implementation. Apparatus 3500 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate biological vital signs.

In some implementations, apparatus 3500 includes a forehead skin-pixel-identification module 3402 that identifies pixel-values that are representative of the skin in two or more images 3404. The forehead skin-pixel-identification module 3402 performs block 4302 in FIG. 43. Some implementations of the forehead skin-pixel-identification module 3402 performs an automatic seed point based clustering process on the images 3404.

In some implementations, apparatus 3500 includes a frequency filter 3406 that receives the output of the forehead skin-pixel-identification module 3402 and applies a frequency filter to the output of the forehead skin-pixel-identification module 3402. The frequency filter 3406 performs block 4304 in FIG. 43 to process the images 3404 in the frequency domain.

In some implementations, apparatus 3500 includes a regional facial clusterial module 3408 that includes a spatial clusterer that is applied to the output of the frequency filter 3406. The regional facial clusterial module 3408 performs block 4306 in FIG. 43. In some implementations the regional facial clusterial module 3408 includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's apparatus or seed point based clustering.

In some implementations, apparatus 3500 includes a frequency-filter 3410 that applies a frequency filter to the output of the regional facial clusterial module 3408, to generate a temporal variation. The frequency-filter 3410 performs block 4308 in FIG. 43. In some implementations, the frequency-filter 3410 is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter. Some implementations of frequency-filter 3410 includes de-noising (e.g. smoothing of the data with a Gaussian filter). The forehead skin-pixel-identification module 3402, the frequency filter 3406, the regional facial clusterial module 3408 and the frequency-filter 3410 amplify temporal variations in the two or more images 3404.

In some implementations, apparatus 3500 includes a biological vital-sign generator 3414 that generates one or more biological vital sign(s) 3416 from the temporal variation. The biological vital sign(s) 3416 are displayed for review by a healthcare worker or stored in a volatile or nonvolatile memory for later analysis, or transmitted to other devices for analysis.

FIG. 36 is a block diagram of an apparatus 3600 of variation amplification, according to an implementation. Apparatus 3600 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate biological vital signs.

In some implementations, apparatus 3600 includes a forehead skin-pixel-identification module 3402 that identifies pixel-values that are representative of the skin in two or more images 3404. The forehead skin-pixel-identification module 3402 performs block 4302 in FIG. 43. Some implementations of the forehead skin-pixel-identification module 3402 performs an automatic seed point based clustering process on the images 3404.

In some implementations, apparatus 3600 includes a spatial bandpass filter 3602 that receives the output of the forehead skin-pixel-identification module 3402 and applies a spatial bandpass filter to the output of the forehead skin-pixel-identification module 3402. The spatial bandpass filter 3602 performs block 4502 in FIG. 45 to process the images 3404 in the spatial domain.

In some implementations, apparatus 3600 includes a regional facial clusterial module 3408 that includes a spatial clusterer that is applied to the output of the frequency filter 3406. In some implementations the regional facial clusterial module 3408 includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's apparatus or seed point based clustering.

In some implementations, apparatus 3600 includes a temporal bandpass filter 3604 that applies a frequency filter to the output of the regional facial clusterial module 3408. The temporal bandpass filter 3604 performs block 4506 in FIG. 45. In some implementations, the temporal bandpass filter 3604 is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter. Some implementations of temporal bandpass filter 3604 includes de-noising (e.g. smoothing of the data with a Gaussian filter).

The forehead skin-pixel-identification module 3402, the spatial bandpass filter 3602, the regional facial clusterial module 3408 and the temporal bandpass filter 3604 amplify temporal variations in the two or more images 3404.

In some implementations, apparatus 3600 includes a temporal-variation identifier 3412 that identifies temporal variation of the output of the frequency-filter 3410. Thus, the temporal variation represents temporal variation of the images 3404. The temporal-variation identifier 3412 performs block 4310 in FIG. 43 or block 4508 in FIG. 45.

In some implementations, apparatus 3600 includes a biological vital-sign generator 3414 that generates one or more biological vital sign(s) 3416 from the temporal variation. The biological vital sign(s) 3416 are displayed for review by a healthcare worker or stored in a volatile or nonvolatile memory for later analysis, or transmitted to other devices for analysis.

FIG. 37 is a block diagram of an apparatus 3700 of variation amplification, according to an implementation.

In some implementations, apparatus 3700 includes a pixel-examiner 3702 that examines pixel-values of two or more images 3404. The pixel-examiner 3702 performs block, 4402 in FIG. 46.

In some implementations, apparatus 3700 includes a temporal variation determiner 3706 that determines a temporal variation of examined pixel-values. The temporal variation determiner 3706 performs block 4404 in FIG. 46.

In some implementations, apparatus 3700 includes a signal-processor 3708 that applies signal processing to the pixel value temporal variation, generating an amplified-temporal-variation. The signal-processor 3708 performs block 4406 in FIG. 46. The signal processing amplifies the temporal variation, even when the temporal variation is small. In some implementations, the signal processing performed by signal-processor 3708 is temporal bandpass filtering that analyzes frequencies over time. In some implementations, the signal processing performed by signal-processor 3708 is spatial processing that removes noise. Apparatus 3700 amplifies only small temporal variations in the signal-processing module.

In some implementations, apparatus 3600 includes a biological vital-sign generator 3414 that generates one or more biological vital sign(s) 3416 from the temporal variation. The biological vital sign(s) 3416 are displayed for review by a healthcare worker or stored in a volatile or nonvolatile memory for later analysis, or transmitted to other devices for analysis.

While apparatus 3700 can process large temporal variations, an advantage in apparatus 3700 is provided for small temporal variations. Therefore apparatus 3700 is most effective when the two or more images 3404 have small temporal variations between the two or more images 3404. In some implementations, a biological vital sign is generated from the amplified-temporal-variations of the two or more images 3404 from the signal-processor 3708.

FIG. 38 is a block diagram of an apparatus 3800 of variation amplification, according to an implementation. Apparatus 3800 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate biological vital signs.

In some implementations, apparatus 3800 includes a forehead-skin pixel identification module 3802 that identifies pixel-values 3806 that are representative of the skin in two or more images 3804. The forehead-skin pixel identification module 3802 performs block 4302 in FIG. 43. Some implementations of the forehead-skin pixel identification module 3802 perform an automatic seed point based clustering process on the two images 3804.

In some implementations, apparatus 3800 includes a frequency-filter module 3808 that receives the identified pixel-values 3806 that are representative of the skin and applies a frequency filter to the identified pixel-values 3806. The frequency-filter module 3808 performs block 4304 in FIG. 43 to process the images 3404 in the frequency domain. Each of the images 3404 is Fourier transformed, multiplied with a filter function and then re-transformed into the spatial domain. Frequency filtering is based on the Fourier Transform. The operator receives the images 3404 and a filter function in the Fourier domain. The images 3404 are then multiplied with the filter function in a pixel-by-pixel fashion using the formula: G(k,l)=F(k,l)H(k,l)

where F(k,l) is the image of identified pixel-values 3806 in the Fourier domain, H(k,l) the filter function and G(k,l) is the frequency filtered identified pixel-values of skin 3810. To obtain the resulting image in the spatial domain, G(k,l) is re-transformed using the inverse Fourier Transform. In some implementations, the frequency-filter module 3808 is a two-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter.

In some implementations, apparatus 3800 includes a spatial-cluster module 3812 that includes a spatial clusterer that is applied to the frequency filtered identified pixel-values of skin 3810, generating spatial clustered frequency filtered identified pixel-values of skin 3814. The spatial-cluster module 3812 performs block 4306 in FIG. 43. In some implementations the spatial-cluster module 3812 includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's apparatus or seed point based clustering.

In some implementations, apparatus 3800 includes a frequency-filter module 3816 that applies a frequency filter to the spatial clustered frequency filtered identified pixel-values of skin 3814, which generates frequency filtered spatial clustered frequency filtered identified pixel-values of skin 3818. The frequency-filter module 3816 performs block 4308 in FIG. 43. In some implementations, the frequency-filter module 3816 is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter. Some implementations of frequency-filter module 3816 includes de-noising (e.g. smoothing of the data with a Gaussian filter).

The forehead-skin pixel identification module 3802, the frequency-filter module 3808, the spatial-cluster module 3812 and the frequency-filter module 3816 amplify temporal variations in the two or more images 3404.

In some implementations, apparatus 3800 includes a temporal-variation module 3820 that determines temporal variation 3822 of the frequency filtered spatial clustered frequency filtered identified pixel-values of skin 3818. Thus, temporal variation 3822 represents temporal variation of the images 3404. The temporal-variation module 3820 performs block 4310 in FIG. 43.

FIG. 39 is a block diagram of an apparatus 3900 to generate and present any one of a number of biological vital signs from amplified motion, according to an implementation.

In some implementations, apparatus 3900 includes a blood-flow-analyzer module 3902 that analyzes a temporal variation to generate a pattern of flow of blood 3904. One example of the temporal variation is temporal variation 3822 in FIG. 38. In some implementations, the pattern flow of blood 3904 is generated from motion changes in the pixels and the temporal variation of color changes in the skin of the images 3404. In some implementations, apparatus 3900 includes a blood-flow display module 3906 that displays the pattern of flow of blood 3904 for review by a healthcare worker.

In some implementations, apparatus 3900 includes a heartrate-analyzer module 3908 that analyzes the temporal variation to generate a heartrate 3910. In some implementations, the heartrate 3910 is generated from the frequency spectrum of the temporal signal in a frequency range for heart beats, such as (0-10 Hertz). In some implementations, apparatus 3900 includes a heartrate display module 3912 that displays the heartrate 3910 for review by a healthcare worker.

In some implementations, apparatus 3900 includes a respiratory rate-analyzer module 3914 that analyzes the temporal variation to determine a respiratory rate 3916. In some implementations, the respiratory rate 3916 is generated from the motion of the pixels in a frequency range for respiration (0-5 Hertz). In some implementations, apparatus 3900 includes respiratory rate display module 3918 that displays the respiratory rate 3916 for review by a healthcare worker.

In some implementations, apparatus 3900 includes a blood-pressure analyzer module 3920 that analyzes the temporal variation to a generate blood pressure 3922. In some implementations, the blood-pressure analyzer module 3920 generates the blood pressure 3922 by analyzing the motion of the pixels and the color changes based on a clustering process and potentially temporal data. In some implementations, apparatus 3900 includes a blood pressure display module 3924 that displays the blood pressure 3922 for review by a healthcare worker.

In some implementations, apparatus 3900 includes an EKG analyzer module 3926 that analyzes the temporal variation to generate an EKG 3928. In some implementations, apparatus 3900 includes an EKG display module 3930 that displays the EKG 3928 for review by a healthcare worker.

In some implementations, apparatus 3900 includes a pulse oximetry analyzer module 3932 that analyzes the temporal variation to generate pulse oximetry 3934. In some implementations, the pulse oximetry analyzer module 3932 generates the pulse oximetry 3934 by analyzing the temporal color changes based in conjunction with the k-means clustering process and potentially temporal data. In some implementations, apparatus 3900 includes a pulse oximetry display module 3936 that displays the pulse oximetry 3934 for review by a healthcare worker.

FIG. 40 is a block diagram of an apparatus 4000 of variation amplification, according to an implementation. Apparatus 4000 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate biological vital signs.

In some implementations, apparatus 4000 includes a forehead-skin pixel identification module 3802 that identifies pixel-values 3806 that are representative of the skin in two or more images 3404. The forehead-skin pixel identification module 3802 performs block 4302 in FIG. 43. Some implementations of the forehead-skin pixel identification module 3802 perform an automatic seed point based clustering process on the images 3404.

In some implementations, apparatus 4000 includes a frequency-filter module 3808 that receives the identified pixel-values 3806 that are representative of the skin and applies a frequency filter to the identified pixel-values 3806. The frequency-filter module 3808 performs block 4304 in FIG. 43 to process the images 3404 in the frequency domain. Each of the images 3404 is Fourier transformed, multiplied with a filter function and then re-transformed into the spatial domain. Frequency filtering is based on the Fourier Transform. The apparatus 4000 takes the images 3404 and a filter function in the Fourier domain. The images 3404 are then multiplied with the filter function in a pixel-by-pixel fashion using the formula: G(k,l)=F(k,l)H(k,l)

where F(k,l) is each of the images 3404 of identified pixel-values 3806 in the Fourier domain, H(k,l) the filter function and G(k,l) is the frequency filtered identified pixel-values of skin 3810. To obtain the resulting image in the spatial domain, G(k,l) is re-transformed using the inverse Fourier Transform. In some implementations, the frequency-filter module 3808 is a two-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter.

In some implementations, apparatus 4000 includes a spatial-cluster module 3812 that includes a spatial clusterer that is applied to the frequency filtered identified pixel-values of skin 3810, generating spatial clustered frequency filtered identified pixel-values of skin 3814. The spatial-cluster module 3812 performs block 4306 in FIG. 43. In some implementations the spatial clustering includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's apparatus or seed point based clustering.

In some implementations, apparatus 4000 includes a frequency-filter module 3816 that applies a frequency filter to the spatial clustered frequency filtered identified pixel-values of skin 3814, which generates frequency filtered spatial clustered frequency filtered identified pixel-values of skin 3818. The frequency-filter module 3816 performs block 4308 in FIG. 43 to generate a temporal variation 3822. In some implementations, the frequency-filter module 3816 is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter. Some implementations of the frequency-filter module 3816 includes de-noising (e.g. smoothing of the data with a Gaussian filter). The forehead-skin pixel identification module 3802, the frequency-filter module 3808, the spatial-cluster module 3812 and the frequency-filter module 3816 amplify temporal variations in the two or more images 3404.

The frequency-filter module 3816 is operably coupled to one or more modules in FIG. 39 to generate and present any one or a number of biological vital signs from amplified motion in the temporal variation 3822.

FIG. 41 is a block diagram of an apparatus 4100 of variation amplification, according to an implementation. Apparatus 4100 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate biological vital signs.

In some implementations, apparatus 4100 includes a forehead-skin pixel identification module 3802 that identifies pixel-values 3806 that are representative of the skin in two or more images 3404. The forehead-skin pixel identification module 3802 performs block 4302 in FIG. 45. Some implementations of the forehead-skin pixel identification module 3802 perform an automatic seed point based clustering process on the images 3404. In some implementations, apparatus 4100 includes a spatial bandpass filter module 4102 that applies a spatial bandpass filter to the identified pixel-values 3806, generating spatial bandpassed filtered identified pixel-values of skin 4104. In some implementations, the spatial bandpass filter module 4102 includes a two-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter. The spatial bandpass filter module 4102 performs block 4502 in FIG. 45.

In some implementations, apparatus 4100 includes a spatial-cluster module 3812 that includes a spatial clusterer that is applied to the frequency filtered identified pixel-values of skin 3810, generating spatial clustered spatial bandpassed identified pixel-values of skin 4106. In some implementations the spatial clustering includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's apparatus or seed point based clustering. The spatial-cluster module 3812 performs block 4504 in FIG. 45.

In some implementations, apparatus 4100 includes a temporal bandpass filter module 4108 that applies a temporal bandpass filter to the spatial clustered spatial bandpass filtered identified pixel-values of skin 4106, generating temporal bandpass filtered spatial clustered spatial bandpass filtered identified pixel-values of skin 4110. In some implementations, the temporal bandpass filter is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter. The temporal bandpass filter module 4108 performs block 4506 in FIG. 45.

In some implementations, apparatus 4100 includes a temporal-variation module 3820 that determines temporal variation 4222 of the temporal bandpass filtered spatial clustered spatial bandpass filtered identified pixel-values of skin 4110. Thus, temporal variation 4222 represents temporal variation of the images 3404. The temporal-variation module 4220 performs block 4508 of FIG. 45. The temporal-variation module 4220 is operably coupled to one or more modules in FIG. 39 to generate and present any one of a number of biological vital signs from amplified motion in the temporal variation 4222.

FIG. 42 is a block diagram of an apparatus 4200 of variation amplification, according to an implementation.

In some implementations, apparatus 4200 includes a pixel-examination-module 4202 that examines pixel-values of two or more images 3404, generating examined pixel-values 4204. The pixel-examination-module 4202 performs block 4602 in FIG. 46.

In some implementations, apparatus 4200 includes a temporal variation determiner module 4206 that determines a temporal variation 4208 of the examined pixel-values 4204. The temporal variation determiner module 4206 performs block 4604 in FIG. 46.

In some implementations, apparatus 4200 includes a signal-processing module 4210 that applies signal processing to pixel values of the temporal variations 4208, generating an amplified temporal variation 4222. The signal-processing module 4210 performs block 4606 in FIG. 46. The signal processing amplifies the temporal variation 4208, even when the temporal variation 4208 is small. In some implementations, the signal processing performed by signal-processing module 4210 is temporal bandpass filtering that analyzes frequencies over time. In some implementations, the signal processing performed by signal-processing module 4210 is spatial processing that removes noise. Apparatus 4200 amplifies only small temporal variations in the signal-processing module.

While apparatus 4200 can process large temporal variations, an advantage in apparatus 4200 is provided for small temporal variations. Therefore apparatus 4200 is most effective when the two or more images 3404 have small temporal variations between the two or more images 3404. In some implementations, a biological vital sign is generated from the amplified-temporal-variations of the two or more images 3404 from the signal-processing module 4210.

8. Biological Vital Sign Amplification Methods

FIG. 43-47 each use spatial and temporal signal processing to generate biological vital signs from a series of digital images.

FIG. 43 is a flowchart of a method 4300 of variation amplification, according to an implementation. Method 4300 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate biological vital signs.

In some implementations, method 4300 includes identifying pixel-values of two or more images that are representative of the skin, at block 4302. Some implementations of identifying pixel-values that are representative of the skin includes performing an automatic seed point based clustering process on the least two images.

In some implementations, method 4300 includes applying a frequency filter to the identified pixel-values that are representative of the skin, at block 4304. In some implementations, the frequency filter in block 4304 is a two-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter.

In some implementations, method 4300 includes applying spatial clustering to the frequency filtered identified pixel-values of skin, at block 4306. In some implementations the spatial clustering includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's method or seed point based clustering.

In some implementations, method 4300 includes applying a frequency filter to the spatial clustered frequency filtered identified pixel-values of skin, at block 4308. In some implementations, the frequency filter in block 4308 is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter. Some implementations of applying a frequency filter at block 4308 include de-noising (e.g. smoothing of the data with a Gaussian filter).

Actions 4302, 4304, 4306 and 4308 amplify temporal variations in the two or more images.

In some implementations, method 4300 includes determining temporal variation of the frequency filtered spatial clustered frequency filtered identified pixel-values of skin, at block 4310.

In some implementations, method 4300 includes analyzing the temporal variation to generate a pattern of flow of blood, at block 4312. In some implementations, the pattern flow of blood is generated from motion changes in the pixels and the temporal variation of color changes in the skin. In some implementations, method 4300 includes displaying the pattern of flow of blood for review by a healthcare worker, at block 4313.

In some implementations, method 4300 includes analyzing the temporal variation to generate heartrate, at block 4314. In some implementations, the heartrate is generated from the frequency spectrum of the temporal variation in a frequency range for heart beats, such as (0-10 Hertz). In some implementations, method 4300 includes displaying the heartrate for review by a healthcare worker, at block 4315.

In some implementations, method 4300 includes analyzing the temporal variation to determine respiratory rate, at block 4316. In some implementations, the respiratory rate is generated from the motion of the pixels in a frequency range for respiration (0-5 Hertz). In some implementations, method 4300 includes displaying the respiratory rate for review by a healthcare worker, at block 4317.

In some implementations, method 4300 includes analyzing the temporal variation to generate blood pressure, at block 4318. In some implementations, the blood pressure is generated by analyzing the motion of the pixels and the color changes based on the clustering process and potentially temporal data from the infrared sensor. In some implementations, method 4300 includes displaying the blood pressure for review by a healthcare worker, at block 4319.

In some implementations, method 4300 includes analyzing the temporal variation to generate EKG, at block 4320. In some implementations, method 4300 includes displaying the EKG for review by a healthcare worker, at block 4321.

In some implementations, method 4300 includes analyzing the temporal variation to generate pulse oximetry, at block 4322. In some implementations, the pulse oximetry is generated by analyzing the temporal color changes based in conjunction with the k-means clustering process and potentially temporal data from the infrared sensor. In some implementations, method 4300 includes displaying the pulse oximetry for review by a healthcare worker, at block 4323.

FIG. 44 is a flowchart of a method of variation amplification, according to an implementation that does not include a separate action of determining a temporal variation. Method 4400 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate biological vital signs.

In some implementations, method 4400 includes identifying pixel-values of two or more images that are representative of the skin, at block 4302. Some implementations of identifying pixel-values that are representative of the skin includes performing an automatic seed point based clustering process on the least two images.

In some implementations, method 4400 includes applying a frequency filter to the identified pixel-values that are representative of the skin, at block 4304. In some implementations, the frequency filter in block 4304 is a two-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter.

In some implementations, method 4400 includes applying spatial clustering to the frequency filtered identified pixel-values of skin, at block 4306. In some implementations the spatial clustering includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's method or seed point based clustering.

In some implementations, method 4400 includes applying a frequency filter to the spatial clustered frequency filtered identified pixel-values of skin, at block 4308, yielding a temporal variation. In some implementations, the frequency filter in block 4308 is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter.

In some implementations, method 4400 includes analyzing the temporal variation to generate a pattern of flow of blood, at block 4312. In some implementations, the pattern flow of blood is generated from motion changes in the pixels and the temporal variation of color changes in the skin. In some implementations, method 4400 includes displaying the pattern of flow of blood for review by a healthcare worker, at block 4313.

In some implementations, method 4400 includes analyzing the temporal variation to generate heartrate, at block 4314. In some implementations, the heartrate is generated from the frequency spectrum of the temporal variation in a frequency range for heart beats, such as (0-10 Hertz). In some implementations, method 4400 includes displaying the heartrate for review by a healthcare worker, at block 4315.

In some implementations, method 4400 includes analyzing the temporal variation to determine respiratory rate, at block 4316. In some implementations, the respiratory rate is generated from the motion of the pixels in a frequency range for respiration (0-5 Hertz). In some implementations, method 4400 includes displaying the respiratory rate for review by a healthcare worker, at block 4317.

In some implementations, method 4400 includes analyzing the temporal variation to generate blood pressure, at block 4318. In some implementations, the blood pressure is generated by analyzing the motion of the pixels and the color changes based on the clustering process and potentially temporal data from the infrared sensor. In some implementations, method 4400 includes displaying the blood pressure for review by a healthcare worker, at block 4319.

In some implementations, method 4400 includes analyzing the temporal variation to generate EKG, at block 4320. In some implementations, method 4400 includes displaying the EKG for review by a healthcare worker, at block 4321.

In some implementations, method 4400 includes analyzing the temporal variation to generate pulse oximetry, at block 4322. In some implementations, the pulse oximetry is generated by analyzing the temporal color changes based in conjunction with the k-means clustering process and potentially temporal data from the infrared sensor. In some implementations, method 4400 includes displaying the pulse oximetry for review by a healthcare worker, at block 4323.

In some implementations, method 4400 includes analyzing the temporal variation to calculate skin perfusion (e.g. blood flow through the skin) to assess a predisposition to skin cancer. Changes in a skin perfusion are thought to be a precursor to skin cancer.

FIG. 45 is a flowchart of a method 4500 of variation amplification from which to generate and communicate biological vital signs, according to an implementation. Method 4500 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate the biological vital signs.

In some implementations, method 4500 includes identifying pixel-values of two or more images that are representative of the skin, at block 4302. Some implementations of identifying pixel-values that are representative of the skin includes performing an automatic seed point based clustering process on the least two images.

In some implementations, method 4500 includes applying a spatial bandpass filter to the identified pixel-values, at block 4502. In some implementations, the spatial filter in block 4502 is a two-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter.

In some implementations, method 4500 includes applying spatial clustering to the spatial bandpass filtered identified pixel-values of skin, at block 4504. In some implementations the spatial clustering includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's method or seed point based clustering.

In some implementations, method 4500 includes applying a temporal bandpass filter to the spatial clustered spatial bandpass filtered identified pixel-values of skin, at block 4506. In some implementations, the temporal bandpass filter in block 4506 is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter.

In some implementations, method 4500 includes determining temporal variation of the temporal bandpass filtered spatial clustered spatial bandpass filtered identified pixel-values of skin, at block 4508.

In some implementations, method 4500 includes analyzing the temporal variation to generate and visually display a pattern of flow of blood, at block 4312. In some implementations, the pattern flow of blood is generated from motion changes in the pixels and the temporal variation of color changes in the skin. In some implementations, method 4500 includes displaying the pattern of flow of blood for review by a healthcare worker, at block 4313.

In some implementations, method 4500 includes analyzing the temporal variation to generate heartrate, at block 4314. In some implementations, the heartrate is generated from the frequency spectrum of the temporal variation in a frequency range for heart beats, such as (0-10 Hertz). In some implementations, method 4500 includes displaying the heartrate for review by a healthcare worker, at block 4315.

In some implementations, method 4500 includes analyzing the temporal variation to determine respiratory rate, at block 4316. In some implementations, the respiratory rate is generated from the motion of the pixels in a frequency range for respiration (0-5 Hertz). In some implementations, method 4500 includes displaying the respiratory rate for review by a healthcare worker, at block 4317.

In some implementations, method 4500 includes analyzing the temporal variation to generate blood pressure, at block 4318. In some implementations, the blood pressure is generated by analyzing the motion of the pixels and the color changes based on the clustering process and potentially temporal data from the infrared sensor. In some implementations, method 4500 includes displaying the blood pressure for review by a healthcare worker, at block 4319.

In some implementations, method 4500 includes analyzing the temporal variation to generate EKG, at block 4320. In some implementations, method 4500 includes displaying the EKG for review by a healthcare worker, at block 4321.

In some implementations, method 4500 includes analyzing the temporal variation to generate pulse oximetry, at block 4322. In some implementations, the pulse oximetry is generated by analyzing the temporal color changes based in conjunction with the k-means clustering process and potentially temporal data from the infrared sensor. In some implementations, method 4500 includes displaying the pulse oximetry for review by a healthcare worker, at block 4323.

FIG. 46 is a flowchart of a method 4600 of variation amplification, according to an implementation. Method 4600 displays the temporal variations based on temporal variations in videos that are difficult or impossible to see with the naked eye. Method 4600 applies spatial decomposition to a video, and applies temporal filtering to the frames. The resulting signal is then amplified to reveal hidden information. Method 4600 can visualize flow of blood filling a face in the video and also amplify and reveal small motions, and other biological vital signs such as blood pressure, skin perfusion, respiration, EKG and pulse. Method 4600 can execute in real time to show phenomena occurring at temporal frequencies selected by the operator. A combination of spatial and temporal processing of videos can amplify subtle variations that reveal important aspects of the world. Method 4600 considers a time series of color values at any spatial location (e.g., a pixel) and amplifies variation in a given temporal frequency band of interest. For example, method 4600 selects and then amplifies a band of temporal frequencies including plausible human heart rates. The amplification reveals the variation of redness as blood flows through the face. Lower spatial frequencies are temporally filtered (spatial pooling) to allow a subtle input signal to rise above the solid-state image transducer 528 and quantization noise. The temporal filtering approach not only amplifies color variation, but can also reveal low-amplitude motion.

Method 4600 can enhance the subtle motions around the chest of a breathing baby. Method 4600 mathematical analysis employs a linear approximation related to the brightness constancy assumption used in optical flow formulations. Method 4600 also derives the conditions under which the linear approximation holds. The derivation leads to a multiscale approach to magnify motion without feature tracking or motion estimation. Properties of a voxel of fluid are observed, such as pressure and velocity, which evolve over time. Method 4600 studies and amplifies the variation of pixel-values over time, in a spatially-multiscale manner. The spatially-multiscale manner to motion magnification does not explicitly estimate motion, but rather exaggerates motion by amplifying temporal color changes at fixed positions. Method 4600 employs differential approximations that form the basis of optical flow processes. Method 4600 described herein employs localized spatial pooling and bandpass filtering to extract and reveal visually the signal corresponding to the pulse. The domain analysis allows amplification and visualization of the pulse signal at each location on the face. Asymmetry in facial blood flow can be a symptom of arterial problems.

Method 4600 described herein makes imperceptible motions visible using a multiscale approach. Method 4600 amplifies small motions, in one implementation. Nearly invisible changes in a dynamic environment can be revealed through spatio-temporal processing of standard monocular video sequences. Moreover, for a range of amplification values that is suitable for various applications, explicit motion estimation is not required to amplify motion in natural videos. Method 4600 is well suited to small displacements and lower spatial frequencies. Single framework can amplify both spatial motion and purely temporal changes (e.g., a heart pulse) and can be adjusted to amplify particular temporal frequencies. A spatial decomposition module decomposes the input video into different spatial frequency bands, then applies the same temporal filter to the spatial frequency bands. The outputted filtered spatial bands are then amplified by an amplification factor, added back to the original signal by adders, and collapsed by a reconstruction module to generate the output video. The temporal filter and amplification factors can be tuned to support different applications. For example, the system can reveal unseen motions of a solid-state image transducer 528, caused by the flipping mirror during a photo burst.

Method 4600 combines spatial and temporal processing to emphasize subtle temporal changes in a video. Method 4600 decomposes the video sequence into different spatial frequency bands. These bands might be magnified differently because (a) the bands might exhibit different signal-to-noise ratios or (b) the bands might contain spatial frequencies for which the linear approximation used in motion magnification does not hold. In the latter case, method 4600 reduces the amplification for these bands to suppress artifacts. When the goal of spatial processing is to increase temporal signal-to-noise ratio by pooling multiple pixels, the method spatially low-pass filters the frames of the video and downsamples the video frames for computational efficiency. In the general case, however, method 4600 computes a full Laplacian pyramid.

Method 4600 then performs temporal processing on each spatial band. Method 4600 considers the time series corresponding to the value of a pixel in a frequency band and applies a bandpass filter to extract the frequency bands of interest. As one example, method 4600 may select frequencies within the range of 0.4-4 Hz, corresponding to 24-240 beats per minute, if the operator wants to magnify a pulse. If method 4600 extracts the pulse rate, then method 4600 can employ a narrow frequency band around that value. The temporal processing is uniform for all spatial levels and for all pixels within each level. Method 4600 then multiplies the extracted bandpassed signal by a magnification factor .alpha. The magnification factor .alpha. can be specified by the operator, and can be attenuated automatically. Method 4600 adds the magnified signal to the original signal and collapses the spatial pyramid to obtain the final output. Since natural videos are spatially and temporally smooth, and since the filtering is performed uniformly over the pixels, the method implicitly maintains spatiotemporal coherency of the results. The motion magnification amplifies small motion without tracking motion. Temporal processing produces motion magnification, shown using an analysis that relies on the first-order Taylor series expansions common in optical flow analyses.

Method 4600 begins with a pixel-examination module in the controller 820 of a MPSB or the microprocessor 2102 of examining pixel-values of two or more images 3404 from the solid-state image transducer 2128, at block 4602.

Method 4600 thereafter determines the temporal variation of the examined pixel-values, at block 4604 by a temporal-variation module in the microprocessor 2102.

A signal-processing module in the microprocessor 2102 applies signal processing to the pixel value temporal variations, at block 4606. Signal processing amplifies the determined temporal variations, even when the temporal variations are small. Method 4600 amplifies only small temporal variations in the signal-processing module. While method 4600 can be applied to large temporal variations, an advantage in method 4600 is provided for small temporal variations. Therefore method 4600 is most effective when the images 3404 have small temporal variations between the images 3404. In some implementations, the signal processing at block 4606 is temporal bandpass filtering that analyzes frequencies over time. In some implementations, the signal processing at block 4606 is spatial processing that removes noise.

In some implementations, a biological vital sign is generated from the amplified-temporal-variations of the images 3404 from the signal processor at block 4608. Examples of generating a biological vital signal from a temporal variation include as in actions 4312, 4314, 4316, 4318, 4320 and 4322 in FIGS. 43, 44 and 45.

FIG. 47 is a flowchart of a method 4700 of variation amplification from which to generate and communicate biological vital signs, according to an implementation. Method 4700 analyzes the temporal and spatial variations in digital images of an animal subject in order to generate and communicate the biological vital signs.

In some implementations, method 4700 includes cropping plurality of images to exclude areas that do not include a skin region, at block 4702. For example, the excluded area can be a perimeter area around the center of each image, so that an outside border area of the image is excluded. In some implementations of cropping out the border, about 72% of the width and about 72% of the height of each image is cropped out, leaving only 7.8% of the original uncropped image, which eliminates about 11/12 of each image and reduces the amount of processing time for the remainder of the actions in this process by about 12-fold. This one action alone at block 4702 in method 4700 can reduce the processing time of the plurality of images 2130 in comparison to method 4500 from 4 minutes to 32 seconds, which is of significant difference to the health workers who used devices that implement method 4700. In some implementations, the remaining area of the image after cropping in a square area and in other implementation the remaining area after cropping is a circular area. Depending upon the topography and shape of the area in the images that has the most pertinent portion of the imaged subject, different geometries and sizes are most beneficial. The action of cropping the images at block 4702 can be applied at the beginning of methods 4300, 4400, 4500 and 4600 in FIGS. 43, 44, 45 and 46, respectively. In other implementations of apparatus 3400, 3500, 3600, 3700, 3800, 3900, 4000, 4100 and 4200, a cropper module that performs block 4702 is placed at the beginning of the modules to greatly decrease processing time of the apparatus.

In some implementations, method 4700 includes identifying pixel-values of the plurality of or more cropped images that are representative of the skin, at block 4704. Some implementations of identifying pixel-values that are representative of the skin include performing an automatic seed point based clustering process on the least two images.

In some implementations, method 4700 includes applying a spatial bandpass filter to the identified pixel-values, at block 4502. In some implementations, the spatial filter in block 4502 is a two-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter.

In some implementations, method 4700 includes applying spatial clustering to the spatial bandpass filtered identified pixel-values of skin, at block 4504. In some implementations the spatial clustering includes fuzzy clustering, k-means clustering, expectation-maximization process, Ward's method or seed point based clustering.

In some implementations, method 4700 includes applying a temporal bandpass filter to the spatial clustered spatial bandpass filtered identified pixel-values of skin, at block 4506. In some implementations, the temporal bandpass filter in block 4506 is a one-dimensional spatial Fourier Transform, a high pass filter, a low pass filter, a bandpass filter or a weighted bandpass filter.

In some implementations, method 4700 includes determining temporal variation of the temporal bandpass filtered spatial clustered spatial bandpass filtered identified pixel-values of skin, at block 4508.

In some implementations, method 4700 includes analyzing the temporal variation to generate and visually display a pattern of flow of blood, at block 4312. In some implementations, the pattern flow of blood is generated from motion changes in the pixels and the temporal variation of color changes in the skin. In some implementations, method 4700 includes displaying the pattern of flow of blood for review by a healthcare worker, at block 4313.

In some implementations, method 4700 includes analyzing the temporal variation to generate heartrate, at block 4314. In some implementations, the heartrate is generated from the frequency spectrum of the temporal variation in a frequency range for heart beats, such as (0-10 Hertz). In some implementations, method 4700 includes displaying the heartrate for review by a healthcare worker, at block 4315.

In some implementations, method 4700 includes analyzing the temporal variation to determine respiratory rate, at block 4316. In some implementations, the respiratory rate is generated from the motion of the pixels in a frequency range for respiration (0-5 Hertz). In some implementations, method 4700 includes displaying the respiratory rate for review by a healthcare worker, at block 4317.

In some implementations, method 4700 includes analyzing the temporal variation to generate blood pressure, at block 4318. In some implementations, the blood pressure is generated by analyzing the motion of the pixels and the color changes based on the clustering process and potentially temporal data from the infrared sensor. In some implementations, method 4700 includes displaying the blood pressure for review by a healthcare worker, at block 4319.

In some implementations, method 4700 includes analyzing the temporal variation to generate EKG, at block 4320. In some implementations, method 4700 includes displaying the EKG for review by a healthcare worker, at block 4321.

In some implementations, method 4700 includes analyzing the temporal variation to generate pulse oximetry, at block 4322. In some implementations, the pulse oximetry is generated by analyzing the temporal color changes based in conjunction with the k-means clustering process and potentially temporal data from the infrared sensor. In some implementations, method 4700 includes displaying the pulse oximetry for review by a healthcare worker, at block 4323.

9. Non-Touch Body Core Temperature Correlation Table Methods

FIG. 48 is a flowchart of a method 4800 to estimate a body core temperature from an external source point in reference to a body core temperature correlation table, according to an implementation.

Method 4800 includes receiving from a non-touch electromagnetic sensor a numerical representation of electromagnetic energy of the external source point of a subject, at block 4802.

Method 4800 also includes estimating the body core temperature of the subject from the numerical representation of the electromagnetic energy of the external source point, a representation of an ambient air temperature reading, a representation of a calibration difference, and a representation of a bias in consideration of the temperature sensing mode, at block 4804. The estimating at block 4804 is based on a body core temperature correlation table representing the body core temperature and the numerical representation of the electromagnetic energy of the external source point.

A body core temperature correlation table provides best results because a linear or a quadratic relationship provides inaccurate estimates of body core temperature, yet a quartic relationship, a quintic relationship, sextic relationship, a septic relationship or an octic relationship provide estimates along a highly irregular curve that is far too wavy or twisting with relatively sharp deviations.

Method 4800 also includes displaying the body core temperature, at block 4806.

FIG. 49 is a flowchart of a method 4900 to estimate a body core temperature from an external source point and other measurements in reference to a body core temperature correlation table, according to an implementation;

Method 4900 includes receiving from a non-touch electromagnetic sensor a numerical representation of electromagnetic energy of the external source point of a subject, at block 4802.

Method 4900 also includes estimating the body core temperature of the subject from the numerical representation of the electromagnetic energy of the external source point, a representation of an ambient air temperature reading, a representation of a calibration difference, and a representation of a bias in consideration of the temperature sensing mode, at block 4902. The estimating at block 4904 is based on a body core temperature correlation table representing three thermal ranges between the body core temperature and the numerical representation of the electromagnetic energy of the external source point.

Method 4900 also includes displaying the body core temperature, at block 4806.

In some implementations, methods 4300-4900 are implemented as a sequence of instructions which, when executed by a microprocessor 2102 in FIG. 21-23, main processor 5002 in FIG. 50, cause the processor to perform the respective method. In other implementations, methods 4300-4900 are implemented as a computer-accessible medium having computer executable instructions capable of directing a microprocessor, such as microprocessor 2102 in FIG. 21-23 or main processor 5002 in FIG. 50, to perform the respective method. In different implementations, the medium is a magnetic medium, an electronic medium, or an optical medium.

Hardware and Operating Environments

FIG. 50 is a block diagram of a multi-vital-sign capture system 5000, according to an implementation. The multi-vital-sign capture system 5000 includes a number of modules such as a main processor 5002 that controls the overall operation of the multi-vital-sign capture system 5000. Communication functions, including data and voice communications, can be performed through a communication subsystem 2146. The communication subsystem 2146 receives messages from and sends messages to wireless networks 5005. In other implementations of the multi-vital-sign capture system 5000, the communication subsystem 2146 can be configured in accordance with the Global System for Mobile Communication (GSM), General Packet Radio Services (GPRS), Enhanced Data GSM Environment (EDGE), Universal Mobile Telecommunications Service (UMTS), data-centric wireless networks, voice-centric wireless networks, and dual-mode networks that can support both voice and data communications over the same physical base stations. Combined dual-mode networks include, but are not limited to, Code Division Multiple Access (CDMA) or CDMA2000 networks, GSM/GPRS networks (as mentioned above), and future third-generation (3G) networks like EDGE and UMTS. Some other examples of data-centric networks include Mobitex™ and DataTAC™ network communication systems. Examples of other voice-centric data networks include Personal Communication Systems (PCS) networks like GSM and Time Division Multiple Access (TDMA) systems.

The wireless link connecting the communication subsystem 2146 with the wireless network 5005 represents one or more different Radio Frequency (RF) channels. With newer network protocols, these channels are capable of supporting both circuit switched voice communications and packet switched data communications.

The main processor 5002 also interacts with additional subsystems such as a Random Access Memory (RAM) 5006, a flash memory 5008, a display 5010, an auxiliary input/output (I/O) subsystem 5012, a data port 5014, a keyboard 5016, a speaker 5018, a microphone 5020, short-range communications subsystem 5022 and other device subsystems 5024. The other device subsystems 5024 can include any one of the pressure sensor 2138, the pressure cuff 2140, the micro dynamic light scattering (mDLS) sensor 2142 and/or the photoplethysmogram (PPG) sensor 2144 that provide signals to the biological vital sign generator 5049. In some implementations, the flash memory 5008 includes a hybrid femtocell/WiFi® protocol stack 5009. The hybrid femtocell/WiFi® protocol stack 5009 supports authentication and authorization between the multi-vital-sign capture system 5000 into a shared WiFi® network and both a 3G, 4G or 5G mobile networks.

Some of the subsystems of the multi-vital-sign capture system 5000 perform communication-related functions, whereas other subsystems may provide “resident” or on-device functions. By way of example, the display 5010 and the keyboard 5016 may be used for both communication-related functions, such as entering a text message for transmission over the wireless network 5005, and device-resident functions such as a calculator or task list.

The multi-vital-sign capture system 5000 can transmit and receive communication signals over the wireless network 5005 after required network registration or activation procedures have been completed. Network access is associated with a subscriber or user of the multi-vital-sign capture system 5000. To identify a subscriber, the multi-vital-sign capture system 5000 requires a SIM card/RUIM 5026 (i.e. Subscriber Identity Module or a Removable User Identity Module) to be inserted into a SIM/RUIM interface 5028 in order to communicate with a network. The SIM card/RUIM or 5026 is one type of a conventional “smart card” that can be used to identify a subscriber of the multi-vital-sign capture system 5000 and to personalize the multi-vital-sign capture system 5000, among other things. Without the SIM card/RUIM 5026, the multi-vital-sign capture system 5000 is not fully operational for communication with the wireless network 5005. By inserting the SIM card/RUIM 5026 into the SIM/RUIM interface 5028, a subscriber can access all subscribed services. Services may include: web browsing and messaging such as e-mail, voice mail, Short Message Service (SMS), and Multimedia Messaging Services (MMS). More advanced services may include: point of sale, field service and sales force automation. The SIM card/RUIM 5026 includes a processor and memory for storing information. Once the SIM card/RUIM 5026 is inserted into the SIM/RUIM interface 5028, the SIM is coupled to the main processor 5002. In order to identify the subscriber, the SIM card/RUIM 5026 can include some user parameters such as an International Mobile Subscriber Identity (IMSI). An advantage of using the SIM card/RUIM 5026 is that a subscriber is not necessarily bound by any single physical mobile device. The SIM card/RUIM 5026 may store additional subscriber information for the multi-vital-sign capture system 5000 as well, including datebook (or calendar) information and recent call information. Alternatively, user identification information can also be programmed into the flash memory 5008.

The multi-vital-sign capture system 5000 is a battery-powered device and includes a battery interface 5032 for receiving one or more batteries 5030. In one or more implementations, the battery 5030 can be a smart battery with an embedded microprocessor. The battery interface 5032 is coupled to a regulator 5033, which assists the battery 5030 in providing power V+ to the multi-vital-sign capture system 5000. Although current technology makes use of a battery, future technologies such as micro fuel cells may provide the power to the multi-vital-sign capture system 5000.

The multi-vital-sign capture system 5000 also includes an operating system 5034 and modules 5036 to 5049 which are described in more detail below. The operating system 5034 and the modules 5036 to 5049 that are executed by the main processor 5002 are typically stored in a persistent nonvolatile medium such as the flash memory 5008, which may alternatively be a read-only memory (ROM) or similar storage element (not shown). Those skilled in the art will appreciate that portions of the operating system 5034 and the modules 5036 to 5049, such as specific device applications, or parts thereof, may be temporarily loaded into a volatile store such as the RAM 5006. Other modules can also be included.

The subset of modules 5036 that control basic device operations, including data and voice communication applications, will normally be installed on the multi-vital-sign capture system 5000 during its manufacture. Other modules include a message application 5038 that can be any suitable module that allows a user of the multi-vital-sign capture system 5000 to transmit and receive electronic messages. Various alternatives exist for the message application 5038 as is well known to those skilled in the art. Messages that have been sent or received by the user are typically stored in the flash memory 5008 of the multi-vital-sign capture system 5000 or some other suitable storage element in the multi-vital-sign capture system 5000. In one or more implementations, some of the sent and received messages may be stored remotely from the multi-vital-sign capture system 5000 such as in a data store of an associated host system with which the multi-vital-sign capture system 5000 communicates.

The modules can further include a device state module 5040, a Personal Information Manager (PIM) 5042, and other suitable modules (not shown). The device state module 5040 provides persistence, i.e. the device state module 5040 ensures that important device data is stored in persistent memory, such as the flash memory 5008, so that the data is not lost when the multi-vital-sign capture system 5000 is turned off or loses power.

The PIM 5042 includes functionality for organizing and managing data items of interest to the user, such as, but not limited to, e-mail, contacts, calendar events, voice mails, appointments, and task items. A PIM application has the ability to transmit and receive data items via the wireless network 5005. PIM data items may be seamlessly integrated, synchronized, and updated via the wireless network 5005 with the multi-vital-sign capture system 5000 subscriber's corresponding data items stored and/or associated with a host computer system. This functionality creates a mirrored host computer on the multi-vital-sign capture system 5000 with respect to such items. This can be particularly advantageous when the host computer system is the multi-vital-sign capture system 5000 subscriber's office computer system.

The multi-vital-sign capture system 5000 also includes a connect module 5044, and an IT policy module 5046. The connect module 5044 implements the communication protocols that are required for the multi-vital-sign capture system 5000 to communicate with the wireless infrastructure and any host system, such as an enterprise system, with which the multi-vital-sign capture system 5000 is authorized to interface. Examples of a wireless infrastructure and an enterprise system are given in FIGS. 50 and 49, which are described in more detail below.

The connect module 5044 includes a set of APIs that can be integrated with the multi-vital-sign capture system 5000 to allow the multi-vital-sign capture system 5000 to use any number of services associated with the enterprise system. The connect module 5044 allows the multi-vital-sign capture system 5000 to establish an end-to-end secure, authenticated communication pipe with the host system. A subset of applications for which access is provided by the connect module 5044 can be used to pass IT policy commands from the host system to the multi-vital-sign capture system 5000. This can be done in a wireless or wired manner. These instructions can then be passed to the IT policy module 5046 to modify the configuration of the multi-vital-sign capture system 5000. Alternatively, in some cases, the IT policy update can also be done over a wired connection.

The IT policy module 5046 receives IT policy data that encodes the IT policy. The IT policy module 5046 then ensures that the IT policy data is authenticated by the multi-vital-sign capture system 5000. The IT policy data can then be stored in the RAM 5006 in its native form. After the IT policy data is stored, a global notification can be sent by the IT policy module 5046 to all of the applications residing on the multi-vital-sign capture system 5000. Applications for which the IT policy may be applicable then respond by reading the IT policy data to look for IT policy rules that are applicable.

The IT policy module 5046 can include a parser 5047, which can be used by the applications to read the IT policy rules. In some cases, another module or application can provide the parser. Grouped IT policy rules, described in more detail below, are retrieved as byte streams, which are then sent (recursively) into the parser to determine the values of each IT policy rule defined within the grouped IT policy rule. In one or more implementations, the IT policy module 5046 can determine which applications are affected by the IT policy data and transmit a notification to only those applications. In either of these cases, for applications that are not being executed by the main processor 5002 at the time of the notification, the applications can call the parser or the IT policy module 5046 when the applications are executed to determine if there are any relevant IT policy rules in the newly received IT policy data.

All applications that support rules in the IT Policy are coded to know the type of data to expect. For example, the value that is set for the “WEP User Name” IT policy rule is known to be a string; therefore the value in the IT policy data that corresponds to this rule is interpreted as a string. As another example, the setting for the “Set Maximum Password Attempts” IT policy rule is known to be an integer, and therefore the value in the IT policy data that corresponds to this rule is interpreted as such.

After the IT policy rules have been applied to the applicable applications or configuration files, the IT policy module 5046 sends an acknowledgement back to the host system to indicate that the IT policy data was received and successfully applied.

The programs 5037 can also include a temporal-variation-amplifier 5048 and a biological vital sign generator 5049. In some implementations, the temporal-variation-amplifier 5048 includes a forehead skin-pixel-identification module 3402, a frequency filter 3406, a regional facial clusterial module 3408 and a frequency filter 3410 as in FIGS. 34 and 35. In some implementations, the temporal-variation-amplifier 5048 includes a forehead skin-pixel-identification module 3402, a spatial bandpass filter 3602, regional facial clusterial module 3408 and a temporal bandpass filter 3604 as in FIG. 36. In some implementations, the temporal-variation-amplifier 5048 includes a pixel-examiner 3702, a temporal variation determiner 3706 and signal processor 3708 as in FIG. 37. In some implementations, the temporal-variation-amplifier 5048 includes a forehead-skin pixel identification module 3802, a frequency-filter module 3808, spatial-cluster module 3812 and a frequency filter module 3816 as in FIGS. 38 and 39. In some implementations, the forehead-skin pixel identification module 3802, a spatial bandpass filter module 4102, a spatial-cluster module 3812 and a temporal bandpass filter module 4106 as in FIG. 41. In some implementations, the temporal-variation-amplifier 5048 includes a pixel-examination-module 4202, a temporal variation determiner module 4206 and a signal processing module 4210 as in FIG. 42. The solid-state image transducer 2128 captures images 2130 and the biological vital sign generator 5049 generates the biological vital sign(s) 3416 that is displayed by display 5010 or transmitted by communication subsystem 2146 or short-range communications subsystem 5022, enunciated by speaker 5018 or stored by flash memory 5008.

Other types of modules can also be installed on the multi-vital-sign capture system 5000. These modules can be third party modules, which are added after the manufacture of the multi-vital-sign capture system 5000. Examples of third party applications include games, calculators, utilities, etc.

The additional applications can be loaded onto the multi-vital-sign capture system 5000 through of the wireless network 5005, the auxiliary I/O subsystem 5012, the data port 5014, the short-range communications subsystem 5022, or any other suitable device subsystem 5024. This flexibility in application installation increases the functionality of the multi-vital-sign capture system 5000 and may provide enhanced on-device functions, communication-related functions, or both. For example, secure communication applications may enable electronic commerce functions and other such financial transactions to be performed using the multi-vital-sign capture system 5000.

The data port 5014 enables a subscriber to set preferences through an external device or module and extends the capabilities of the multi-vital-sign capture system 5000 by providing for information or module downloads to the multi-vital-sign capture system 5000 other than through a wireless communication network. The alternate download path may, for example, be used to load an encryption key onto the multi-vital-sign capture system 5000 through a direct and thus reliable and trusted connection to provide secure device communication.

The data port 5014 can be any suitable port that enables data communication between the multi-vital-sign capture system 5000 and another computing device. The data port 5014 can be a serial or a parallel port. In some instances, the data port 5014 can be a USB port that includes data lines for data transfer and a supply line that can provide a charging current to charge the battery 5030 of the multi-vital-sign capture system 5000.

The short-range communications subsystem 5022 provides for communication between the multi-vital-sign capture system 5000 and different systems or devices, without the use of the wireless network 5005. For example, the short-range communications subsystem 5022 may include an infrared device and associated circuits and modules for short-range communication. Examples of short-range communication standards include standards developed by the Infrared Data Association (IrDA), Bluetooth®, and the 802.11 family of standards developed by IEEE.

Bluetooth® is a wireless technology standard for exchanging data over short distances (using short-wavelength radio transmissions in the ISM band from 2400-2480 MHz) from fixed and mobile devices, creating personal area networks (PANs) with high levels of security. Created by telecom vendor Ericsson in 1994, Bluetooth® was originally conceived as a wireless alternative to RS-232 data cables. Bluetooth® can connect several devices, overcoming problems of synchronization. Bluetooth® operates in the range of 2400-2483.5 MHz (including guard bands), which is in the globally unlicensed Industrial, Scientific and Medical (ISM) 2.4 GHz short-range radio frequency band. Bluetooth® uses a radio technology called frequency-hopping spread spectrum. The transmitted data is divided into packets and each packet is transmitted on one of the 79 designated Bluetooth® channels. Each channel has a bandwidth of 1 MHz. The first channel starts at 2402 MHz and continues up to 2480 MHz in 1 MHz steps. The first channel usually performs 1600 hops per second, with Adaptive Frequency-Hopping (AFH) enabled. Originally Gaussian frequency-shift keying (GFSK) modulation was the only modulation scheme available; subsequently, since the introduction of Bluetooth® 2.0+EDR, π/4-DQPSK and 8DPSK modulation may also be used between compatible devices. Devices functioning with GFSK are said to be operating in basic rate (BR) mode where an instantaneous data rate of 1 Mbit/s is possible. The term Enhanced Data Rate (EDR) is used to describe π/4-DPSK and 8DPSK schemes, each giving 2 and 3 Mbit/s respectively. The combination of these (BR and EDR) modes in Bluetooth® radio technology is classified as a “BR/EDR radio”. Bluetooth® is a packet-based protocol with a master-slave structure. One master may communicate with up to 7 slaves in a piconet; all devices share the master's clock. Packet exchange is based on the basic clock, defined by the master, which ticks at 452.5 μs intervals. Two clock ticks make up a slot of 625 μs; two slots make up a slot pair of 1250 μs. In the simple case of single-slot packets the master transmits in even slots and receives in odd slots; the slave, conversely, receives in even slots and transmits in odd slots. Packets may be 1, 3 or 5 slots long but in all cases the master transmit will begin in even slots and the slave transmit in odd slots. A master Bluetooth® device can communicate with a maximum of seven devices in a piconet (an ad-hoc computer network using Bluetooth® technology), though not all devices reach this maximum. The devices can switch roles, by agreement, and the slave can become the master (for example, a headset initiating a connection to a phone will necessarily begin as master, as initiator of the connection; but may subsequently prefer to be slave). The Bluetooth® Core Specification provides for the connection of two or more piconets to form a scatternet, in which certain devices simultaneously play the master role in one piconet and the slave role in another. At any given time, data can be transferred between the master and one other device (except for the little-used broadcast mode. The master chooses which slave device to address; typically, the master switches rapidly from one device to another in a round-robin fashion. Since the master chooses which slave to address, whereas a slave is (in theory) supposed to listen in each receive slot, being a master is a lighter burden than being a slave. Being a master of seven slaves is possible; being a slave of more than one master is difficult. Many of the services offered over Bluetooth® can expose private data or allow the connecting party to control the Bluetooth® device. For security reasons it is necessary to be able to recognize specific devices and thus enable control over which devices are allowed to connect to a given Bluetooth® device. At the same time, it is useful for Bluetooth® devices to be able to establish a connection without user intervention (for example, as soon as the Bluetooth® devices of each other are in range). To resolve this conflict, Bluetooth® uses a process called bonding, and a bond is created through a process called pairing. The pairing process is triggered either by a specific request from a user to create a bond (for example, the user explicitly requests to “Add a Bluetooth® device”), or the pairing process is triggered automatically when connecting to a service where (for the first time) the identity of a device is required for security purposes. These two cases are referred to as dedicated bonding and general bonding respectively. Pairing often involves some level of user interaction; this user interaction is the basis for confirming the identity of the devices. Once pairing successfully completes, a bond will have been formed between the two devices, enabling those two devices to connect to each other in the future without requiring the pairing process in order to confirm the identity of the devices. When desired, the bonding relationship can later be removed by the user. Secure Simple Pairing (SSP): This is required by Bluetooth® v2.1, although a Bluetooth® v2.1 device may only use legacy pairing to interoperate with a v2.0 or earlier device. Secure Simple Pairing uses a form of public key cryptography, and some types can help protect against man in the middle, or MITM attacks. SSP has the following characteristics: Just works: As implied by the name, this method just works. No user interaction is required; however, a device may prompt the user to confirm the pairing process. This method is typically used by headsets with very limited IO capabilities, and is more secure than the fixed PIN mechanism which is typically used for legacy pairing by this set of limited devices. This method provides no man in the middle (MITM) protection. Numeric comparison: If both devices have a display and can accept a binary Yes/No user input, both devices may use Numeric Comparison. This method displays a 6-digit numeric code on each device. The user should compare the numbers to ensure that the numbers are identical. If the comparison succeeds, the user(s) should confirm pairing on the device(s) that can accept an input. This method provides MITM protection, assuming the user confirms on both devices and actually performs the comparison properly. Passkey Entry: This method may be used between a device with a display and a device with numeric keypad entry (such as a keyboard), or two devices with numeric keypad entry. In the first case, the display is used to show a 6-digit numeric code to the user, who then enters the code on the keypad. In the second case, the user of each device enters the same 6-digit number. Both of these cases provide MITM protection. Out of band (OOB): This method uses an external means of communication, such as Near Field Communication (NFC) to exchange some information used in the pairing process. Pairing is completed using the Bluetooth® radio, but requires information from the OOB mechanism. This provides only the level of MITM protection that is present in the OOB mechanism. SSP is considered simple for the following reasons: In most cases, SSP does not require a user to generate a passkey. For use-cases not requiring MITM protection, user interaction can be eliminated. For numeric comparison, MITM protection can be achieved with a simple equality comparison by the user. Using OOB with NFC enables pairing when devices simply get close, rather than requiring a lengthy discovery process.

In use, a received signal such as a text message, an e-mail message, or web page download will be processed by the communication subsystem 2146 and input to the main processor 5002. The main processor 5002 will then process the received signal for output to the display 5010 or alternatively to the auxiliary I/O subsystem 5012. A subscriber may also compose data items, such as e-mail messages, for example, using the keyboard 5016 in conjunction with the display 5010 and possibly the auxiliary I/O subsystem 5012. The auxiliary I/O subsystem 5012 may include devices such as: a touch screen, mouse, track ball, infrared fingerprint detector, or a roller wheel with dynamic button pressing capability. The keyboard 5016 is preferably an alphanumeric keyboard and/or telephone-type keypad. However, other types of keyboards may also be used. A composed item may be transmitted over the wireless network 5005 through the communication subsystem 2146.

For voice communications, the overall operation of the multi-vital-sign capture system 5000 is substantially similar, except that the received signals are output to the speaker 5018, and signals for transmission are generated by the microphone 5020. Alternative voice or audio I/O subsystems, such as a voice message recording subsystem, can also be implemented on the multi-vital-sign capture system 5000. Although voice or audio signal output is accomplished primarily through the speaker 5018, the display 5010 can also be used to provide additional information such as the identity of a calling party, duration of a voice call, or other voice call related information.

FIG. 51 is a block diagram of a solid-state image transducer 5100, according to an implementation. The solid-state image transducer 5100 includes a great number of photoelectric elements, a.sub.1..sub.1, a.sub.2..sub.1, . . . , a.sub.mn, in the minute segment form, transfer gates TG1, TG2, . . . TGn responsive to a control pulse V.sub.φP for transferring the charges stored on the individual photoelectric elements as an image signal to vertical shift registers VS1, VS2, . . . , VSn, and a horizontal shift register HS for transferring the image signal from the vertical shift registers VSs, through a buffer amplifier 2 d to an outlet 2 e. After the one-frame image signal is stored, the image signal is transferred to vertical shift register by the pulse V.sub.φP and the contents of the vertical shift registers VSs are transferred upward line by line in response to a series of control pulses V.sub.φV1, V.sub.φV2. During the time interval between the successive two vertical transfer control pulses, the horizontal shift register HS responsive to a series of control pulses V.sub.φH1, V.sub.φH2 transfers the contents of the horizontal shift registers HSs in each line row by row to the right as viewed in FIG. 51. As a result, the one-frame image signal is formed by reading out the outputs of the individual photoelectric elements in such order.

FIG. 52 is a block diagram of the wireless communication subsystem 2146, according to an implementation. The wireless communication subsystem 2146 includes a receiver 5200, a transmitter 5202, as well as associated components such as one or more embedded or antennas 5204 and 5206, Local Oscillators (LOs) 5208, and a processing module such as a digital signal processor (DSP) 5210. The particular implementation of the wireless communication subsystem 2146 is dependent upon communication protocols of a wireless network 5205 with which the mobile device is intended to operate. Thus, it should be understood that the implementation illustrated in FIG. 52 serves only as one example. Examples of the multi-vital-sign capture system 444 include multi-vital-sign capture system 5000, multi-vital-sign capture system in FIGS. 4-8 and 7-13, apparatus that estimates a body core temperature 21-24, apparatus of variation amplification FIG. 34-42 and multi-vital-sign capture system 5000. Examples of the wireless network 5205 include network 5005 in FIG. 50.

Signals received by the antenna 5204 through the wireless network 5205 are input to the receiver 5200, which may perform such common receiver functions as signal amplification, frequency down conversion, filtering, channel selection, and analog-to-digital (A/D) conversion. A/D conversion of a received signal allows more complex communication functions such as demodulation and decoding to be performed in the DSP 5210. In a similar manner, signals to be transmitted are processed, including modulation and encoding, by the DSP 5210. These DSP-processed signals are input to the transmitter 5202 for digital-to-analog (D/A) conversion, frequency up conversion, filtering, amplification and transmission over the wireless network 5205 via the antenna 5206. The DSP 5210 not only processes communication signals, but also provides for receiver and transmitter control. For example, the gains applied to communication signals in the receiver 5200 and the transmitter 5202 may be adaptively controlled through automatic gain control algorithms implemented in the DSP 5210.

The wireless link between the multi-vital-sign capture system(s) 104 and the wireless network 5205 can contain one or more different channels, typically different RF channels, and associated protocols used between the multi-vital-sign capture system(s) 104 and the wireless network 5205. An RF channel is a limited resource that must be conserved, typically due to limits in overall bandwidth and limited battery power of the multi-vital-sign capture system(s) 104.

When the multi-vital-sign capture system(s) 104 are fully operational, the transmitter 5202 is typically keyed or turned on only when it is transmitting to the wireless network 5205 and is otherwise turned off to conserve resources. Similarly, the receiver 5200 is periodically turned off to conserve power until the receiver 5200 is needed to receive signals or information (if at all) during designated time periods.

The PMR 103 is received by the wireless communication subsystem 2146 from the main processor 5002 at the DSP 5210 and then transmitted to the wireless network 5205 through the antenna 5204 of the receiver 5200.

FIG. 53 is a block diagram of a Non-Contact Human Multi-Vital Sign (NCPMVS) device 5300, according to an implementation. NCPMVS 5300 is one implementation of NCPMVS 404 in FIG. 4. The NCPMVS 5300 includes a sensor printed circuit board (PCB) 5302. The sensor PCB 5302 includes proximity sensors 5304, 5306 and 5308, and temperature sensor 5310, autofocus lens 5312 in front of camera sensor 5314 and an illumination light emitting diode (LED) 5316. The includes proximity sensors 5304, 5306 and 5308 are operably coupled to a first I²C port 5318 of a microprocessor 5320. One example of the microprocessor 5320 is a Qualcomm Snapdragon microprocessor chipset. The temperature sensor 5310 is operably coupled to a second I²C port 5322 of the microprocessor 5320. The I²C standard is a multi-master, multi-slave, single-ended, serial computer bus developed by Philips Semiconductor (now NXP Semiconductors) for attaching lower-speed peripheral ICs to processors and microcontrollers in short-distance, intra-board communication. The camera sensor 5314 is operably coupled to a MIPI port 5324 of the microprocessor 5320. The MIPI standard is defined by the MIPI standard is defined by the MIPI Alliance, Inc. of Piscataway, N.J. The a MIPI port 5324 is also operably coupled to a MIPI RGB bridge 5326, and the MIPI RGB bridge 5326 is operably coupled to a display device 5328 such as a TFT Color Display (2.8″). The illumination LED 5316 is operably coupled to a pulse-width modulator (PWM) 5330 of the microprocessor 5320. The PWM 5330 is also operably coupled to a haptic motor 5332. The microprocessor 5320 also includes a GPIO port 5334, the GPIO port 5334 being a general-purpose input/output that is a generic pin on an integrated circuit or computer board whose behavior—including whether GPIO port 5334 is an input or output pin—is controllable by the microprocessor 5320 at run time. The GPIO port 5334 is operably coupled to a keyboard 5336, such as a membrane keypad (3× buttons). The microprocessor 5320 is also operably coupled to an audio codec 5338 with is operably coupled to a speaker 5340. The microprocessor 5320 also includes a Bluetooth® communication port 5342 and a WiFi® communication port 5344, that are both capable of communicating with a PCB antenna 5346. The microprocessor 5320 is also operably coupled to a micro SD slot (for debugging purposes), a flash memory unit 5350, a DDR3 random access memory unit 5352 and a micro USB port 5354 (for debugging purposes). The micro USB port 5354 is operably coupled to voltage rails and a battery power/management component 5358. The battery power/management component 5358 is operably coupled to a battery 5360, which is operably coupled to a charger connector 5362.

FIG. 54-61 are drawings of various views of a multi-vital-sign finger cuff, according to an implementation. SPO2 subsystem 5402 in FIG. 54-61 is one example of the SPO2 subsystem 418. Finger occlusion cuff 5404 in FIG. 54-61 is one example of the finger occlusion cuff 416. mDLS sensor(s) 6102 is the same as in the multi-vital-sign finger cuff 506 in FIGS. 5-7, 844 and 846 in FIG. 8, and/or 2142. PPG sensor 6104 is the same as in the PPG sensor 806 in FIG. 8 and the PPG sensor 2144 in FIG. 21.

FIG. 62-68 are drawings of various views of a multi-vital-sign capture system 6200, according to an implementation. The multi-vital-sign capture system 6200 includes a multi-vital-sign finger cuff 5400 that is operably to a base 6202, and the base 6202 is operably coupled to a Non-Contact Human Multi-Vital Sign (NCPMVS) device 6204. The NCPMVS device 6204 is one example of the NCPMVS device 404. The multi-vital-sign finger cuff 5400 is shown in greater detail in FIG. 54-61. The multi-vital-sign finger cuff 5400 includes a SPO2 subsystem 5402 and a finger occlusion cuff 5404. The SPO2 subsystem 5402 and the finger occlusion cuff 5404 are shown in greater detail in FIG. 54-61. FIG. 67 shows an ECG subsystem 6702 that includes a plurality of ECG sensors 6704, 6706 and/or 6708. The ECG sensors 6704, 6706 and/or 6708 are either ‘wet’ sensors that require use of a gel or the ECG sensors 6704, 6706 and/or 6708 are ‘dry’ sensors that do not require use of a gel. The wet ECG sensors 6704, 6706 and/or 6708 are fabricated by coating a plastic injection molded substrate with a very thin layer of silver and the outer layer of the silver is converted to silver chloride. The dry ECG sensors 6704, 6706 and/or 6708 are fabricated with a dry conductive composite. Conductive carbon fiber loaded ABS plastic can be used to reduce silver and eliminate stainless steel, brass, and nickel used in electrode components. These engineered resins reduce or eliminate corrosion or galvanic reactions. The electrode-skin impedance is governed by contact area and skin properties as well as the materials used in manufacture and presents specific challenges to designers of cost effective disposable electrodes. ECG sensors 6704, 6706 and/or 6708 can also include nano composites, microscopic circuitry, low power wireless and RFID.

FIG. 68 shows a multi-vital-sign capture system 6200 that includes a printed circuit board 6802 that is mounted in the base of the multi-vital-sign capture system 6200 and that is operably coupled to the multi-vital-sign finger cuff 5400. The multi-vital-sign capture system 6200 also includes a non-contact human multi-vital sign device 6204, which is shown in greater detail in FIG. 69. FIG. 69 is an exploded view of a non-contact human multi-vital sign device 6204, according to an implementation. The non-contact human multi-vital sign (NCPMVS) device 6204 is one example of the NCPMVS device 404 in FIG. 4 and the NCPMVS device 503 in FIG. 5.

FIG. 70 is a block diagram of a Multi-Vital Sign (MVS) system 7000, according to an implementation. The MVS system 7000 includes four communicatively coupled devices; a Multi-Parameter Sensor Box (MPSB) 7002, a Non-Contact Human Multi-Vital Sign (NCPMVS) device 7003, a finger sensor assembly (FSA) 7006, and a Multi-Parameter Sensor Box Recharge Station (MPSBRS) 7020. MPSB 7002 is one implementation of MPSB 402 in FIG. 4. NCPMVS 7003 is one implementation of NCPMVS 404 in FIG. 4. The MVS system 7000, the MPSB 7002 and the NCPMVS device 7003 are all examples of the multi-vital-sign capture system(s) 104.

Multi-Parameter Sensor Box (MPSB)

The MPSB includes a pneumatic engine 507 that is mechanically coupled to the finger sensor assembly 7006 and a sensor control and management component 7008.

MPSB 7002 includes a USB port 519 for interface only with the NCPMVS 7003 device to perform the following functions: recharge the internal rechargeable batteries 520 of the MPSB 7002, export sensor data sets to a windows based computer system, firmware update of the MPSB 7002 via an application to control and manage the firmware update of the MPSB 7002 and configuration update of the MPSB 7002. The MPSB 7002 does not update the NCPMVS 7003 device firmware. The MPSB 7002 also includes internal rechargeable batteries 520 that can be recharged via a USB port 522, which provides charge, and the MPSB 7002 also includes an external direct DC input providing a fast recharge. The internal batteries of the MPSB 7002 can be recharged when the MPSB 7002 is powered-off but while connected to USB or DC input. In some implementations, the MPSB 7002 can recharge the NCPMVS 7003 device from its internal power source over a wireless charging connection. In some implementations, the internal rechargeable batteries 520 provide sufficient operational life of the MPSB 7002 on a single charge to perform at least 2 days of full measurements before recharging of the internal rechargeable batteries 520 of the MPSB 7002 is required.

In some implementations, the MPSB 7002 includes an internal non-volatile, non-user removable, data storage device 524 for up to 20 human raw measurement data sets. The data storage device 524 can be removed by a technician when the data storage device 524 is determined to be faulty. A human measurement set contains all measurement data and measurements acquired by the MPSB 7002, including the temperature measurement from the NCPMVS 7003. The internal memory is protected against data corruption in the event of an abrupt power loss event. The MPSB 7002 and the NCPMVS 7003 have a human-form fit function sensor and device industrial/mechanical design. The MPSB 7002 also includes anti-microbial exterior material to and an easy clean surface for all sensor and device surfaces. The MPSB 7002 stores in the data storage device 524 an “atomic” human record structure that contains the entire data set recording for a single human measurement containing all human raw sensor signals and readings, extracted human vitals, and system status information. The MPSB 7002 includes self-test components that determine the operational state of the MPSB 7002 and sub systems, to ensure that the MPSB 7002 is functional for measurement. The MPSB 7002 includes a clock function for date and time. In some implementations. The date and time of the MPSB 7002 is be updated from the NCPMVS 7003. In some implementations, the MPSB 7002 includes user input controls, such as a power on/off switch (start/stop), an emergency stop control to bring the multi-vital-sign finger cuff to a deflated condition. In some implementations, all other input is +supported via the NCPMVS 7003 via on screen information of the NCPMVS 7003. In some implementations, the MPSB 7002 includes visual indicators 526 such as a fatal fault indicator that indicates device has failed and will not power up, a device fault indicator (that indicates the MPSB 7002 has a fault that would affect the measurement function), battery charging status indicator, battery charged status indicator, a battery fault status indicator.

The components (e.g. 507, 513, 519, 520, 522, 524, 526 and 7008) in the MPSB 7002 are controlled by a control process component 7010. The control process component 7010 can be implemented by a microprocessor or by a FPGA.

The MPSB 7002 is hand held and portable, weighing no more than 0.2 Kg. In other implementations, that MPSB 7002 has a heavy weight, over 0.5 kg, in order to have mechanical stability on a table. The MPSB 7002 includes non-slip/slide exterior surface material.

Finger Sensor Assembly

The finger sensor assembly 7006 is replaceable, detachable and removable from the MPSB 7002. The finger sensor assembly 7006 includes a front end sensor electronic interface 802 and a front end subject physical interface 804, as described in FIG. 8 The finger pressure cuff 850 in the front end subject physical interface 804 in FIG. 70 is powered via an air line that is a pneumatic tube (e.g. 408 in FIG. 4) by the pneumatic engine 507 in the MPSB 7002 that provides air pressure to inflate a cuff bladder in the finger pressure cuff 850 and the controlled release of that pressure.

In some implementations, the finger sensor assembly 7006 also includes the following sensors and sensor signal capture and processing components: an infrared finger temperature sensor 508 and an ambient temperature sensor 512.

In some implementations, data from the sensors in the finger sensor assembly 7006 is collected and managed by the FSA from which multiple vital signs are generated by the controller 820 in the front-end sensor electronic interface 802 and the generated multiple vital signs are sent through the high speed serial transmission/receive line 7012 to the management component 7019. In other implementations, data from the sensors in the finger sensor assembly 7006 is collected and managed by the MPSB 7002 through a high speed serial transmission/receive line 7012, from which multiple vital signs are generated by a sensor control and a management component 7019.

Power is received by the finger sensor assembly 7006 in a power component 7014 from the MPSB 7002 though a power line 7016. The serial transmission/receive line 7012 receives sensor data from the PPG sensor 806, the mDLS sensor 811, the mDLS sensor 814 and the finger pressure cuff 850 in the front-end sensor electronic interface 802 of the FSA 7006 and the infrared finger temperature sensor 508, the ambient temperature sensor 512 in the FSA 7006. The airline 408, power line 7016 and the high speed serial transmission/receive line 7012 are bundled into a finger sensor cable 7018.

A PPG sensor cover 848 is mechanically coupled to the PPG sensor 806.

Non-Contact Human Multi-Vital Sign (NCPMVS) Device

The NCPMVS 7003 captures, stores and exports raw data from all supported sensors in the system. More specifically, the NCPMVS 7003 extracts and displays vital sign parameters and transfers the parameters to either a remote third party, hub, bridge etc., or a device manager, or directly to remote EMR/HER/Hospital systems or other third party local or cloud based systems. MVS system 7000 provides a flexible human vital sign measurement methodology that supports different measurement methods and techniques. The MVS system 7000 can be used in a clinical setting for the collection of human vital signs.

In some implementations, a single stage measurement process is required to measure all vital signs in one operation by the NCPMVS 7003 by the replaceable, detachable and removable multi-vital-sign finger cuff 406 or the finger sensor assembly 7006 or the infrared finger temperature sensor 508. However, in some implementations, a two stage measurement process is performed in which the MPSB 7002 measures some vital signs through the replaceable, detachable and removable multi-vital-sign finger cuff 406 or the finger sensor assembly 7006; and in the second stage, the body surface temperature is measured through an infrared temperature sensor 508 in the NCPMVS device 7003. One implementation of the infrared finger temperature sensor 508 is digital infrared sensor 2600 in FIG. 26.

The MPSB 7002 operates in two primary modes, the modes of operation based on who takes the measurements, a patient or an operator. The two modes are: 1) Operator Mode in which an operator operates the MPSB 7002 to take a set of vital sign measurements of another human. The operator is typically clinical staff or a home care giver. 2) Patient Mode in which a patient uses the MPSB 7002 to take a set of vital sign measurements of themselves. In some implementations, the MPSB 7002 provides both the main measurement modes for patient and operator. The primary measurement areas on the human to be measured are 1) Left hand, index and middle finger, 2) right hand, index and middle finger, and 3) human forehead temperature (requires the other device to perform temperature measurement). The MPSB 7002 is portable, light weight, hand held and easy to use in primary and secondary modes of operation in all operational environments.

Given the complex nature of integration into hospital networks, in some implementations, in some implementations the MPSB 7002 does not include site communication infrastructure, rather the collected data (vital sign) is extracted from the MPSB 7002 via a USB port or by a USB mass storage stick that is inserted into the MPSB 7002 or by connecting the MPSB 7002 directly to a PC system as a mass storage device itself.

When the NCPMVS device 7003 is connected to a wireless Bluetooth® communication component 513 of the MPSB 7002 via a wireless Bluetooth® communication component 514, is a slave to the MPSB 7002. The NCPMVS 7003 reports status, measurement process, and measurement measurements to the user via the MPSB 7002. The NCPMVS 7003 provides a user input method to the MPSB 7002 via a graphical user interface on a LCD display 515 which displays data representative of the measurement process and status. In one implementation, the wireless Bluetooth® communication component 513 of the MPSB 7002 includes communication capability with wireless communication paths (3G, 4G and/or 5G WiFi®, NFC, Z-wave) communication paths and the MPSB 7002 is not a slave to the NCPMVS 7003. The NCPMVS 7003 captures vital sig data and transmits the vital sign data via the wireless Bluetooth® communication component 513 in the MPSB 7002 to the middle layer 106 in FIG. 1 or the NCPMVS 7003 transmits the vital sign data via the communication component 516 of the NCPMVS 7003 to the bridge 302, the WiFi® access point 304 in FIG. 3, the cellular communications tower 306, the third party bridge 312 in FIG. 3.

In some implementations, the NCPMVS 7003 provides communications with other devices via a communication component 516 of the NCPMVS 7003. The communication component 516 has communication capability with cellular communication paths (3G, 4G and/or 5G) and/or WiFi® communication paths. For example, the MPSB 7002 captures vital sign data and transmits the vital sign data via the wireless Bluetooth® communication component 513 in the MPSB 7002 to the wireless Bluetooth® communication component 514 in the NCPMVS 7003, and the NCPMVS 7003 transmits the vital sign data via the communication component 516 of the NCPMVS 7003 to the middle layer 106 in FIG. 1 or the NCPMVS 7003 transmits the vital sign data via the communication component 516 of the NCPMVS 7003 to the bridge 302, the WiFi® access point 304 in FIG. 3, the cellular communications tower 306, the third party bridge 312 in FIG. 3. The NCPMVS 7003 also includes at least one internal rechargeable battery 517 and user interface keys 518. The infrared finger temperature sensor 508, the ambient temperature sensor 512, wireless Bluetooth® communication component 514, the graphical user interface on a LCD display 515, communication component 516 of the NCPMVS 7003. The at least one internal rechargeable battery 517 and user interface keys 518 are controlled by a main controller (microprocessor) 505.

In some implementations, when the NCPMVS 7003 is connected to the MPSB 7002, the NCPMVS 7003 performs human bar code scan or identification entry as requested by MPSB 7002, the NCPMVS 7003 performs an operator bar code scan or identification entry as requested by MPSB 7002, the NCPMVS 7003 performs human temperature measurement as requested by MPSB 7002, the NCPMVS 7003 displays information that is related to the MPSB 7002 direct action, the NCPMVS 7003 starts when the MPSB 7002 is started, and the NCPMVS 7003 is shutdown under the direction and control of the MPSB 7002, and the NCPMVS 7003 has a self-test mode that determines the operational state of the MPSB 7002 and sub systems, to ensure that the MPSB 7002 is functional for the measurement. In other implementations, when the NCPMVS 7003 is connected to the MPSB 7002, the NCPMVS 7003 performs human bar code scan or identification entry as requested by NCPMVS 7003, the NCPMVS 7003 performs an operator bar code scan or identification entry as requested by NCPMVS 7003, the NCPMVS 7003 performs human temperature measurement as requested by NCPMVS 7003 and the NCPMVS 7003 displays information that is related to the MPSB 7002 direct action. In some implementations, the information displayed by the NCPMVS 7003 includes date/time, human identification number, human name, vitals measurement such as blood pressure (diastolic and systolic), SPO2, heart rate, temperature, respiratory rate, MPSB 7002 free memory slots, battery status of the NCPMVS 7003, battery status of the MPSB 7002, device status of the MPSB 7002, errors of the NCPMVS 7003, device measurement sequence, measurement quality assessment measurement, mode of operation, subject and operator identification, temperature, measurement, display mode and device revision numbers of the NCPMVS 7003 and the MPSB 7002. In some implementations, when a body surface temperature of a human is also sensed by an infrared sensor in the Non-Contact Human Multi-Vital Sign (NCPMVS) device 7003, the body surface temperature is collected and managed by the MPSB 7002. In other implementations, when a body surface temperature of a human is sensed by an infrared sensor in the Non-Contact Human Multi-Vital Sign (NCPMVS) device 7003, the body surface temperature is not collected and managed by the MPSB 7002.

The NCPMVS 7003 device performs concurrent two stage measurement processes for all measurements. The measurement process performed by the NCPMVS 7003 device is controlled and guided from the NCPMVS 7003 device via the GUI on the MPSB 7002. The measurements are sequenced and configured to minimize time required to complete all measurements. In some implementations, the NCPMVS 7003 device calculates the secondary measurements of heart rate variability and blood flow. The NCPMVS 7003 device commands and controls the MPSB 7002 via a wireless Bluetooth® protocol communication line 412 and in some further implementations, the MPSB 7002 communicates to other devices through Bluetooth® protocol communication line (not shown), in addition to the communications with the NCPMVS 7003 device, which could also be concurrent. In some further implementations, the NCPMVS 7003 communicates to other devices through Bluetooth® protocol communication line (not shown), in addition to the communications with the MPSB 7002 device, which could also be concurrent.

NCPMVS 7003 includes a connection status indicator (connected/not connected, fault detected, charging/not charging), a connected power source status indicator, (either USB or DC input) and a power On/Off status indicator. The visual indicators are visible in low light conditions in the home and clinical environment.

In some embodiments, the NCPMVS device 7003 includes a docking apparatus that mechanically and electrically interfaces with the FSA 7006.

Multi-Parameter Sensor Box Recharge Station (MPSBRS) 7020

The Multi-Parameter Sensor Box Recharge Station (MPSBRS) 7020, provides electrical power to recharge the MPSB 7002. The MPSBRS 7020 can provide electrical power to recharge the batteries of the MPSB 7002 either via a physical wired connection or via a wireless charger 530. In some implementations, the MPSBRS 7020 does not provide electrical power to the MPSB 7002 because the MPSB 7002 includes internal rechargeable batteries 520 that can be recharged via either USB port 522 or a DC input.

The MPSBRS 7020 includes a security lock system 532, a LED status indicator 534, a power supply 536, a main alternating current input 538 and MPSB battery recharge controller 540.

FIG. 71 is a block diagram of a multi-parameter sensor box that is operable to couple to a finger sensor assembly, according to an implementation.

MPSB 7100 supports a variety measurement methods and techniques. The MPSB 700 can be used in a clinical setting for the collection of human vital signs in connection with a FSA 7006 in FIG. 70.

MPSB 7100 includes all the components of MPSB 700 in FIG. 7 except a display screen 709, the multi-vital-sign finger cuff 506, the infrared finger temperature sensor 508 and the ambient temperature sensor 512 which are excluded from MPSB 7100.

In MPSB 7100, power is transmitted to a finger sensor assembly 7006 though power line 7016. The finger pressure cuff 850 in the front end subject physical interface 804 in FIG. 70 is powered via an air line (408 in FIG. 71 that is a pneumatic tube) by the pneumatic engine 507 in the MPSB 7002 that provides air pressure to inflate a cuff bladder in the finger pressure cuff 850 and the controlled release of that pressure. The serial transmission/receive line 7012 receives sensor data from the PPG sensor 806, the mDLS sensor 811, the mDLS sensor 814 and the finger pressure cuff 850 in the front-end sensor electronic interface 802 of the FSA 7006 and the infrared finger temperature sensor 508, the ambient temperature sensor 512 in the FSA 7006. The air line 408, power line 7016 and the high speed serial transmission/receive line 7012 are bundled into a finger sensor cable 7018.

FIG. 72 is a block diagram of a front end of a multi-vital-sign finger cuff 7200, according to an implementation.

The front end of a multi-vital-sign finger cuff 7200 is one implementation of a portion of a multi-vital-sign finger cuff 406 in FIG. 4. The front end of a multi-vital-sign finger cuff 7200 captures, stores and exports raw data from all supported sensors in the system. The front end of a multi-vital-sign finger cuff 7200 supports a variety measurement methods and techniques. The front end of a multi-vital-sign finger cuff 7200 can be used in a clinical setting for the collection of human vital signs.

The front end of a multi-vital-sign finger cuff 7200 includes a front-end sensor electronic interface 802 that is mechanically coupled to a front-end subject physical interface 804. The front-end subject physical interface 804 includes a multiplexer 808 that is electrically coupled to a PPG controller 810. The front-end subject physical interface 804 includes to a multiplexer 812 which is electrically coupled to a MDLS controller 813. The front-end sensor electronic interface 802 includes a multiplexer 816 that is electrically coupled to a mDLS controller 817. The front-end sensor electronic interface 802 includes an ambient temperature sensor 512. The front-end sensor electronic interface 802 includes a 3-axis accelerometer 818.

The PPG controller 810 is electrically coupled to a controller 820 through a Serial Peripheral Interface (SPI) 822. The mDLS controller 813 is electrically coupled to the controller 820 through a SPI 824. The mDLS sensor 814 is electrically coupled to the controller 820 through a SPI 826. The ambient temperature sensor 512 is electrically coupled to the controller 820 through a I2C interface 828. The 3-axis accelerometer 818 is electrically coupled to the controller 820 through the I2C interface 828.

Visual indicator(s) 526 are electrically coupled to the controller 820 through a general-purpose input/output (GPIO) interface 830. A serial port 832 and a high speed serial port 834 are electrically coupled to the controller 820 and a serial power interface 836 is electrically coupled to the high speed serial port 834. A voltage regulator 838 is electrically coupled to the controller 820. A sensor front-end test component is electrically coupled to the controller 820 through the GPIO interface 830.

The front-end subject physical interface 804 includes a PPG sensor 806 that is electrically coupled to the multiplexer 808 front-end sensor electronic interface 802. The front-end subject physical interface 804 includes a mDLS sensor 811 that is electrically coupled to the multiplexer 812 in the front-end sensor electronic interface 802. The front-end sensor electronic interface 802 includes a mDLS sensor 814 that is electrically coupled to a multiplexer 816 in the front-end sensor electronic interface 802.

The front-end subject physical interface 804 includes a PPG sensor cover 848 that is mechanically coupled to the PPG sensor 806. The front-end subject physical interface 804 includes a finger pressure cuff 850 that is mechanically coupled to the front-end subject physical interface 804.

The front-end sensor electronic interface 802 includes a pneumatic connector 852 that is mechanically coupled to the finger pressure cuff 850 in the front-end subject physical interface 804 via an air line 408.

FIG. 73 is a block diagram of a multi-vital-sign device in a telemedicine system 7300. Telemedicine is the practice of caring for patients remotely, when the healthcare provider and patient are not physically present with each other. In telemedicine system 7300, the data from the multi-vital-sign capture device 7302 is wirelessly communicated via an encrypted communication channel 7304 to a secure audiovisual communication component 7306 that provides screen sharing and realtime video communications for telemedicine applications between healthcare practitioners and staff and patients, then the data from the multi-vital-sign capture device 7302 is wirelessly communicated via an encrypted communication channel via Bluetooth, WIFI, or cellular transmission to a data hub 7307 and then through a data cloud 7308 and then the data from the multi-vital-sign capture device 7302 is communicated via an encrypted communication channel to a clinical data repository 7310, a cloud electronic medical records (EMR) system 7312 and a clinical monitoring system 7314, such as the Capsule platform that is manufactured by Capsule a Qualcomm Life company at 300 Brickstone Square, Suite 203, Andover, Mass. 01810. Examples of the multi-vital sign-capture device 7302 include Examples of the secure audiovisual communication component 7306 is Vsee by Vsee Corp. of Sunnyvale, Calif., ooVoo by ooVoo LLC of New York City, N.Y. and Google Hangouts by Alphabet Corp. of Mountain View Calif. The telemedicine system 7300 also can include a medical institution 7316, such as a hospital, that is operably coupled to a wide-area network 7318 that is operably coupled to a healthcare data interchange portal component 7320. The medical institution 7316 is operably coupled to an electronic medical record (EMR) system 7322. The data hub 7307 is operably coupled to the data cloud 7308 and then to the clinical data repository 7310, the cloud electronic medical records (EMR) system 7312 and the clinical monitoring system 7314.

FIG. 74 is a block diagram of a multi-vital-sign device in a telemedicine system 7400. In telemedicine system 7400, the data from the multi-vital-sign capture device 7302 is wirelessly communicated via an encrypted communication channel 7304 to a data hub 7307 and then to a HIPPA-compliant data hub 7402. The HIPPA-compliant data hub 7402 transmits the data from the multi-vital-sign capture device 7302 to a multi-vital sign (MVS) predictive analytics engine 7404, a big data artificial intelligence engine 7406, the clinical data repository 7310, the cloud electronic medical records (EMR) system 7312 and the secure audiovisual communication component 7306.

FIG. 75 is a block diagram of a multi-vital-sign device in a telemedicine system 7500. In telemedicine system 7500, the multi-vital-sign device is a Non-Contact Human Multi-Vital Sign (NCPMVS) device 5300, which uses a 3D camera for motion amplification, wound identification and characterization and skin perfusion quantification (predictor of skin cancer). The motion amplification helps determine skin perfusion to quantify blood flow through the skin as a predictor or leading indicator of skin cancer. The NCPMVS device 5300 also includes a reflective SPO2 sensor for non touch SPO2 detection.

The NCPMVS device 5300 transmits data 7502 that represents the motion amplification, the wound identification and characterization and the skin perfusion quantification via a WiFi communication link 7504 to the wide-area network 7318 and via a BlueTooth® communication link 7506 to an IoT hub 7508. The wide-area network 7318 transmits the data 7502 to the data hub 7307. The wide-area network 7318 and the IoT hub 7508 transmits the data 7502 to the healthcare data interchange portal component 7320 and the healthcare data interchange portal component 7320 transmits the data 7502 to the cloud electronic medical records (EMR) system 7312. The IoT hub 7508 is an IoT gateway that connects wired/wireless peripherals, such as the Non-Contact Human Multi-Vital Sign (NCPMVS) device 5300 and securely forwards data from the wired/wireless peripherals. The IoT hub 7508 is also a beacon that is enabled for proximity and location based workflows, and provides IoT triggers that provide context for users, services and facilities. The IoT hub 7508 also provides HDX casting that redirects video output from Mobile device to the IoT hub 7508, supports virtual channels that enable hub keyboard/mouse/peripherals and beacon proximity service enabling mobile authentication with hub session roaming. HDX casting provides a set of capabilities that deliver a “high-definition” experience to users of centralized applications and desktops, on any device and over any network. HDX technologies are built on top of the ICA remoting protocol, proven in large enterprise environments and accessed by millions of users globally. HDX casting is built on top of three technical principles 1) intelligent redirection, 2) adaptive compression and 3) data de-duplication.

FIG. 76 is an isometric drawing of a multi-vital sign-capture device 7600 according to an implementation. The multi-vital sign-capture device 7700 includes a multi-vital-sign finger cuff, such as multi-vital-sign finger cuff 5400 in FIG. 54-61, which includes a SPO2 subsystem 5402, which is shown in greater detail in FIG. 54-61 and which also includes a finger occlusion cuff 5404, which is shown in greater detail in FIG. 54-61. The multi-vital-sign finger cuff 5400 in the multi-vital sign-capture device 7600 is mounted at an angle of 90 degrees to the multi-vital-sign finger cuff 5400 in the multi-vital sign-capture device 6200 in FIG. 62-68. The multi-vital-sign finger cuff 5400 in the multi-vital sign-capture device 7600 includes the SPO2 subsystem 5402 and the finger occlusion cuff 5404. The multi-vital sign-capture device 7600 includes the Non-Contact Human Multi-Vital Sign (NCPMVS) device 5300 that is operably to the SPO2 subsystem 5402 and the finger occlusion cuff 5404.

CONCLUSION

A multi-vital-sign capture system that senses temperature, heart rate at rest, heart rate variability, respiration, SPO2 oxygenation, blood flow and blood pressure through a device, and transmits the vital signs to an electronic medical record system. The device can act as a hub to integrate other vital signs and relevant health care parameters in a hospital, home, or mobile environment. A technical effect of the apparatus and methods disclosed herein is electronic transmission of a body core temperature that is estimated from signals from the non-touch electromagnetic sensor to an electronic medical record system and combination of sensing heart rate at rest, heart rate variability, respiration, SPO2, blood flow and blood pressure. Another technical effect of the apparatus and methods disclosed herein is generating a temporal variation of images from which a biological vital sign can be transmitted to an electronic medical record system. Although specific implementations are illustrated and described herein, it will be appreciated by those of ordinary skill in the art that any arrangement which is generated to achieve the same purpose may be substituted for the specific implementations shown. This application is intended to cover any adaptations or variations. Further implementations of power supply to all devices includes A/C power both as a supplemental power supply to battery power and as a substitute power supply.

In particular, one of skill in the art will readily appreciate that the names of the methods and apparatus are not intended to limit implementations. Furthermore, additional methods and apparatus can be added to the modules, functions can be rearranged among the modules, and new modules to correspond to future enhancements and physical devices used in implementations can be introduced without departing from the scope of implementations. One of skill in the art will readily recognize that implementations are applicable to future vital sign and non-touch temperature sensing devices, different temperature measuring sites on humans or animals, new communication protocols for transmission (of user service, patient service, observation service, and chart service and all current and future application programming interfaces and new display devices.

The terminology used in this application meant to include all temperature sensors, processors and operator environments and alternate technologies which provide the same functionality as described herein. 

The invention claimed is:
 1. A multi-vital sign device comprising: a finger cuff comprising: a photoplethysmogram sensor; a micro dynamic light scattering sensor; a cuff bladder that expands and contracts in response to air pressure; a first circuit board including: a first microprocessor; the first microprocessor operably coupled to the cuff bladder, the photoplethysmogram sensor and the micro dynamic light scattering sensor; and a first digital interface that is operably coupled to the first microprocessor; a pneumatic engine that is mechanically coupled to the cuff bladder via an air line and that supplies the air pressure to the cuff bladder; a non-contact human multi-vital sign device comprising: a housing having a top, two sides, two ends and a bottom and comprising: a second circuit board including: a second digital interface, the second digital interface being operably coupled to the first digital interface; and a second microprocessor operably coupled to the second digital interface, the second microprocessor being configured to estimate a plurality of vital signs from data from the photoplethysmogram sensor, from the micro dynamic light scattering sensor and the cuff bladder; wherein the finger cuff is mounted to the base that is mounted on one of the two sides of the housing of the non-contact human multi-vital sign device.
 2. The multi-vital sign device of claim 1 further comprising a display device that further comprises: a green traffic light that is associated with a first vital sign of the plurality of vital signs and that is configured to indicate that the first vital sign is good; an amber traffic light that is associated with the first vital sign of the plurality of vital signs and that is configured to indicate that the first vital sign is low; and a red traffic light that is associated with the first vital sign of the plurality of vital signs and that is configured to indicate that the first vital sign is high.
 3. The multi-vital sign device of claim 1 further comprising a digital infrared sensor having no analog sensor readout ports.
 4. The multi-vital sign device of claim 1 further comprising: a three-dimensional camera that is operably coupled to the second microprocessor and configured to provide a plurality of images to the second microprocessor; and the first microprocessor including a cropper module that is configured to receive the plurality of images and configured to crop the plurality of images to exclude a border area of the plurality of images, generating a plurality of cropped images, the second microprocessor also including a temporal-variation-amplifier of the plurality of cropped images that is configured to generate a temporal variation, the second microprocessor also including a biological vital sign generator that is operably coupled to the temporal-variation-amplifier that is configured to generate a biological vital sign from the temporal variation, wherein the biological vital sign is one of the plurality of vital signs.
 5. The multi-vital sign device of claim 4, wherein the temporal-variation-amplifier further comprises a skin-pixel-identification module.
 6. The multi-vital sign device of claim 4, wherein the biological vital sign further comprises wound identification and characterization and skin perfusion that quantifies blood flow through skin as a predictor of skin cancer.
 7. The multi-vital sign device of claim 4, wherein the temporal-variation-amplifier further comprises a first frequency filter module.
 8. The multi-vital sign device of claim 4 wherein a heart rate at rest is estimated from data from a photoplethysmogram sensor, a respiration rate and a heart rate variability and a blood pressure diastolic is estimated from data from a micro dynamic light scattering sensor and the photoplethysmogram sensor.
 9. The multi-vital sign device of claim 4 further comprising: wherein a blood pressure systolic is estimated from data from a micro dynamic light scattering sensor.
 10. The multi-vital sign device of claim 4 further comprising a storage device that is operably coupled to the biological vital sign generator and that is configured to store the plurality of vital signs to the multi-vital sign device.
 11. The multi-vital sign device of claim 4 wherein a wireless communication subsystem is operably coupled to the second microprocessor and the wireless communication subsystem is configured to transmit a representation of the biological vital sign via a short distance wireless communication path to an IoT hub that is a beacon that is operable for proximity and location based workflows and provides context for users, services and facilities, supports virtual channels and provides HDX casting that redirects video output from the multi-vital sign device, and provides intelligent redirection, adaptive compression and data duplication.
 12. The multi-vital sign device of claim 11 wherein the multi-vital sign device is verified by a second device as known by the second device and as allowed by the second device to transfer information to the second device.
 13. The multi-vital sign device of claim 11 wherein a connection is established and the plurality of vital signs are pushed from the multi-vital sign device through the wireless communication subsystem, thereafter an external device controls flow of the plurality of vital signs between the multi-vital sign device and the external device, wherein the connection further comprises an encrypted communication channel.
 14. The multi-vital sign device of claim 11, wherein a digital infrared sensor further comprises an analog-to-digital sensor.
 15. The multi-vital sign device of claim 11, wherein the wireless communication subsystem further comprises a component that is configured to transmit a representation of date and time, operator identification, patient identification, manufacturer and model number of the multi-vital sign device. 